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美国
证券交易委员会
华盛顿特区20549
_______________________________________________________
表格 10-Q
_______________________________________________________
根据1934年证券交易法第13或15(d)节的季度报告
截至季度结束日期的财务报告2024年9月30日
或者
根据1934年证券交易法第13或15(d)节的转型报告书
过渡期从             到                
委员会档案号码:
000-50679
_______________________________________________________
CORCEPT THERAPEUTICS INCORPORATED
(公司章程中指定的确切公司名称)
_______________________________________________________
特拉华州77-0487658
(国家或其他管辖区的
公司成立或组织)
(IRS雇主
唯一识别号码)
Redwood Shores Parkway 101号
Redwood City, 加利福尼亚州 94065
(总部地址,包括邮政编码)
_______________________________________________________
(650) 327-3270
(注册人电话号码,包括区号)
_______________________________________________________

根据法案第12(b)条注册的证券:
每一类的名称交易标志在其上注册的交易所的名称
普通股,每股0.001美元面值CORT纳斯达克证券交易所 LLC
请勾选以下选项,以表明要件:(1)在过去12个月内(或在注册者需要提交这些报告的较短时期内)已提交1934年证券交易法13或15(d)节要求提交的所有报告,并且(2)在过去90天内一直需要提交此类报告。  ☒    否  ☐
请用复选标记表示,登记者在过去的12个月中(或者对于登记者需要提交这些文件的更短时期),是否已按照《S-T规定第405条》的规定提交了应提交的每个交互数据文件。  ☒    否  ☐
请勾选标记以说明注册人是大型快速申报人、加速申报人、非加速申报人、较小的报告公司还是新兴成长型公司。请查看《交易所法》第120亿.2条中“大型快速申报人”、“加速申报人”、“较小的报告公司”和“新兴成长型公司”的定义。
大型加速报告人加速文件申报人
非加速文件提交人更小的报告公司
成长型公司
如果是新兴成长公司,请在复核者处标明勾选符号,说明注册者是否选择不使用依据证券交易法第13(a)条规定提供的任何新的或修订后的财务会计准则的扩展过渡期。 ☐
请勾选以下内容。申报人是否是外壳公司(根据证券交易法规则12b-2定义)。    是      否  ☒
2024年10月23日,有 104,775,137 每股面值为$0.001的普通股。




目录

2

第一部分 财务信息
项目1。基本报表
corcept医疗公司
简明合并资产负债表
(以千为单位)
2020年9月30日
2024
12月31日
2023
 (未经审计)(见注1)
资产  
流动资产:  
现金及现金等价物$137,289 $135,551 
短期市场证券243,047 232,670 
应收账款,扣除准备金59,717 41,123 
与Melucci诉讼相关的保险赔款应收款(注4) 14,000 
库存8,050 7,730 
预付费用和其他流动资产18,875 27,562 
总流动资产466,978 458,636 
战略库存7,764 8,244 
经营租赁资产使用权5,503 120 
资产和设备,净值2,930 195 
长期有价证券167,310 57,176 
其他6,973 6,541 
126,799 90,605 
总资产$784,257 $621,517 
负债和股东权益
流动负债:
应付账款$18,584 $17,396 
应计研发费用27,736 21,330 
应计负债及其他负债79,464 51,628 
与Melucci诉讼相关的应计结算(附注4) 14,000 
短期租赁负债432 151 
流动负债合计126,216 104,505 
长期经营租赁负债6,359  
长期应计所得税应付款12,847 10,307 
负债合计145,422 114,812 
承诺和或因应事项(注4)
股东权益:
优先股  
135 133 
自家保管的股票(682,177)(635,078)
额外实收资本806,317 738,515 
累计其他综合收益1,571 609 
保留盈余512,989 402,526 
股东权益总额638,835 506,705 
负债和股东权益总额$784,257 $621,517 
随附说明是这些简明合并财务报表的一部分。
3

corcept医疗公司
简明合并利润表
(未经审计)
(以千为单位,除每股数据外)
截至9月30日的三个月截至9月30日的九个月
 2024202320242023
产品收入,扣除折扣$182,546 $123,601 $493,150 $346,970 
营业费用:
销售成本2,867 1,645 7,926 4,604 
研发59,336 45,517 176,587 129,646 
销售、一般及行政费用73,745 45,262 196,948 137,107 
营业费用总计135,948 92,424 381,461 271,357 
营业利润46,598 31,177 111,689 75,613 
利息和其他收入6,345 5,208 17,844 12,135 
税前收入52,943 36,385 129,533 87,748 
所得税费用(5,730)(5,007)(19,070)(12,963)
净收入47,213 31,378 110,463 74,785 
归属于普通股股东的净收益46,690 31,172 109,344 74,353 
每股基本净利润$0.45 $0.31 $1.06 $0.72 
每股稀释净利润$0.41 $0.28 $0.98 $0.66 
用于计算每股普通股净利润的加权平均股份
基本103,371 102,014 103,094 103,933 
稀释的113,723 111,099 111,571 112,054 
随附说明是这些简明合并财务报表的一部分。
4

corcept医疗公司
综合收益简明合并报表
(未经审计)
(以千为单位)
截至9月30日的三个月截至9月30日的九个月
 2024202320242023
净收入47,213 31,378 110,463 74,785 
其他综合收益(损失):
可供出售投资的未实现收益(损失),减税效果后的净额($256), $31, $(139) and $(184和), 分别为
951 (95)432 586 
外汇翻译收益(损失)536 (184)530 49 
总综合收益$48,700 $31,099 $111,425 $75,420 
相关附注是这些基本报表的一个不可或缺的部分。
5

corcept医疗公司
简明财务报表现金流量表
(未经查核)
(以千为单位)
 截至9月30日的九个月
 20242023
经营活动现金流量:  
净利润$110,463 $74,785 
调整净利润以达经营活动所提供之净现金流量:
股份报酬44,558 35,875 
证券投资折价(溢价)之累积差异(8,747)(5,933)
折旧与摊提514 828 
推延所得税(36,333)(25,821)
租赁权资产摊销362 1,262 
营运资产和负债的变化:
应收贸易款项(18,594)(3,569)
与Melucci诉讼有关的保险索偿应收款项14,000  
存货383 936 
预付费用及其他流动资产8,462 (5,579)
其他资产(432) 
应付账款1,616 4,783 
研发费用已列入费用6,406 6,732 
应计利益及其他负债27,531 36,695 
与Melucci诉讼相关的应计和解(14,000) 
长期应计所得税2,540 1,373 
营业租赁负债38 (1,215)
经营活动产生的净现金流量138,767 121,152 
投资活动之现金流量:
购买不动产和设备(2,051)(139)
来自可销售证券到期所得332,545 372,793 
可销售证券的购入(443,738)(298,846)
投资活动提供的净现金流量(使用)(113,244)73,808 
来自筹资活动的现金流量:
来自股票期权行使的收入,扣除发行成本后的净额3,268 1,091 
员工股票购买计划下的购买收入3,927 2,959 
与股份回购计划相关的普通股回购(15,664) 
在收购要约中回购普通股 (145,428)
支付现金以满足免现金期权行使及受限制股授予的法定扣缴要求(15,316)(8,111)
筹集资金的净现金流量(23,785)(149,489)
现金及现金等价物净增加1,738 45,471 
现金及现金等价物期初余额135,551 66,329 
现金及现金等价物期末余额$137,289 $111,800 

6

补充揭露:
行使回购的股票成本,用于无现金选择权行使的净结算$14,184 $22,199 
相关附注是这些基本报表的一个不可或缺的部分。
7

corcept医疗公司
股东权益简明合并财务报表
(未经查核)
(以千为单位)
普通股额外的
实收资本
资本
库藏股累计
其他
综合
收入(损失)
保留收益总计
股东权益
股权
股份金额
2023年12月31日余额103,405 $133 $738,515 $(635,078)$609 $402,526 $506,705 
根据激励奖计划发行普通股786 — 3,485 — — — 3,485 
股份用于满足现金无偿期权行使及限制股解锁时的成本和法定代扣要求(143)— 2,032 (5,586)— — (3,554)
与股份回购计划相关的普通股回购(20)— — (476)— — (476)
与净股回购相关的奢华税— — — 81 — — 81 
股份报酬— — 12,929 — — — 12,929 
与员工股票购买计划相关的限制股解锁— — 1,283 — — — 1,283 
其他全面损失,扣除税后净额— — — — (351)— (351)
净利润— — — — — 27,762 27,762 
2024年3月31日止结余104,028 $133 $758,244 $(641,059)$258 $430,288 $547,864 
根据激励奖励计划发行普通股份700 1 7,573 — — — 7,574 
股份用于支付现金期权行使和受限股解除的成本和法定代扣要求,以进行无现金结算(208)— — (6,242)— — (6,242)
根据股票回购计划回购普通股份(122)— — (3,478)— — (3,478)
与净股份回购相关的消费税— — — 16 — — 16 
股份报酬— — 13,881 — — — 13,881 
与员工股票购买计划中受限股解除相关的股票颁发— — 1,314 — — — 1,314 
其他全面损失,扣除税后净额— — — — (174)— (174)
净利润— — — — — 35,488 35,488 
2024年6月30日余额104,398 $134 $781,012 $(650,763)$84 $465,776 $596,243 
根据激励奖励计划发行普通股1,175 1 10,321 — — — 10,322 
股份被提供以满足现金期权行使和受限制股解除须支付成本及法定扣缴要求的净结算(526)— — (19,704)— — (19,704)
在股票回购计划中回购普通股(344)— — (11,710)— — (11,710)
股份报酬— — 14,286 — — — 14,286 
受员工股票购买计划之限制性股解除的分配— — 698 — — — 698 
其他综合收益,税后— — — — 1,487 — 1,487 
净利润— — — — — 47,213 47,213 
2024年9月30日结余104,703 $135 $806,317 $(682,177)$1,571 $512,989 $638,835 
相关附注是这些基本报表的一个不可或缺的部分。
8

普通股额外的
实收资本
资本
库藏股累计
其他
综合
收入(损失)
保留收益总计
股东权益
股权
股份金额
2022年12月31日结余107,835 $131 $662,342 $(456,148)$(869)$296,386 $501,842 
根据激励奖励计划发行普通股份618 — 6,540 — — — 6,540 
股份被提供以满足现金无现金选择权行使的成本和法定扣缴要求(297)— — (6,359)— — (6,359)
股份报酬— — 10,966 — — — 10,966 
其他综合收益,税后— — — — 716 — 716 
净利润— — — — — 15,879 15,879 
2023年3月31日结束余额108,156 $131 $679,848 $(462,507)$(153)$312,265 $529,584 
根据激励奖励计划发行普通股份1,168 1 4,496 — — — 4,497 
股份被提供以满足现金无现金选择权行使的成本和法定扣缴要求(202)— — (4,823)— — (4,823)
回购普通股与要约收购相关(6,610)— — (145,428)— — (145,428)
与净利润份额回购相关的货物税— — — (1,316)— — (1,316)
股份报酬— — 11,374 — — — 11,374 
其他综合收益,税后— — — — 198 — 198 
净利润— — — — — 27,528 27,528 
2023年6月30日结余102,512 $132 $695,718 $(614,074)$45 $339,793 $421,614 
在奖励计划下发行普通股1,068 1 13,949 — — — 13,950 
购买股份以满足无现金期权行使的成本和法定代扣需求(584)— — (17,866)— — (17,866)
与净利润分享回购相关的消费税— — — 152 — — 152 
股份报酬— — 11,660 — — — 11,660 
与员工股票认购计划相关的限制性股票授予— — 1,070 — — — 1,070 
其他全面损失,扣除税后净额— — — — (279)— (279)
净利润— — — — — 31,378 31,378 
截至2023年9月30日的结余102,996 $133 $722,397 $(631,788)$(234)$371,171 $461,679 
随附说明是这些简明合并财务报表的一部分。
9

corcept医疗公司
未经审计的缩编合并财务报表附注
1. 报告的编制基于美国公认会计原则(US GAAP)和证券交易委员会(SEC)的适用规则和法规,关于中期财务报告的规定。根据这些规定的规定,某些按照美国公认会计原则通常要求的注脚或其他财务信息已被精简或省略,因此2024年1月31日的资产负债表及相关披露信息已来源于那个日期的经审计合并财务报表,但不包含美国公认会计原则要求的所有信息。这些未经审计的简明合并财务报表与公司的年度合并财务报表基于相同的基础而编制,经管理层的意见,反映了必要的调整(仅包括正常循环调整),以公平呈现公司的简明合并财务信息。2024年4月30日的营业结果不一定是预期的2025年1月31日或任何其他中期或未来年度的结果。
业务说明及基本准则
corcept医疗公司(以下简称“Corcept”,“本公司”,“我们”和“我们的”)是一家从事发现和开发药物治疗严重内分泌、肿瘤、代谢和神经系统疾病的商业阶段药品公司,通过调节激素皮质醇的作用。2012年,美国食品药品监督管理局(“FDA”)批准Korlym®(米非司酮)300毫克片,作为一种每日一次的口服药物,用于治疗因内源性库欣氏综合征导致的高血糖的成人患者,这些患者患有2型糖尿病或葡萄糖不耐受,并且手术失败或不适合手术。2024年6月,我们推出了Korlym的授权通用版本,用于相同适应症。我们已发现并拥有专利的 四个具有结构独特的选择性皮质醇调节剂系列,包括超过1,000化合物。我们正在开发这些系列化合物,作为潜在治疗广泛严重疾病的药物。
我们公司成立于1998年5月份,在加利福尼亚州雷德伍德城设有总部。
报告范围
我们按照美国通用会计准则("GAAP")和《10-Q表格》的指示和《S-X法规》第10条准则准备了以下临时基本报表:(i)截至2024年9月30日的简明综合资产负债表,以及(ii)截至2024年9月30日和2023年的三个和九个月的简明综合收入、综合收益和股东权益表,以及(iii)截至2024年9月30日和2023年的九个月的简明综合现金流量表。这些报表不包括所有基本报表所需的信息和附注。据管理层意见,包括了为了公平呈现所需的所有调整(适用期间仅包括正常、重复性调整)。截至2024年9月30日的三个和九个月的运营结果不一定代表2024年其余时间或其他任何期间的结果。这些基本报表和附注应当与2023年12月31日结束的年度财务报表一并阅读,这些财务报表包含在我们的《10-K表格》年度报告中。2023年12月31日的资产负债表来源于当日的审计基本报表。
重要会计政策的描述在截至2023年12月31日的年度10-k表格中未发生重大变化。
最近发布的未采纳会计准则
2023年12月,财务会计准则委员会(“FASB”)发布了会计准则更新(“ASU”)No. 2023-09,要求报告实体的有效税率调和信息进行细分,以及有关所缴所得税的信息。该准则旨在通过提供更详细的所得税披露,有助于投资者做出资本配置决策。这项ASU适用于在2024年12月15日后年度起的上市公司,允许提前采纳。我们计划在2025年12月31日结束的财政年度采纳这一指引。我们目前正在评估采纳这项指引将对简明一体化财务报表产生的影响。
2023年11月,FASB发布了ASU No. 2023-07,旨在改善关于上市实体可报告部门的披露,并满足投资者对可报告部门费用的额外、更详细信息的要求。该标准适用于年度开始于2023年12月15日后的上市公司,对于2024年12月15日后年度开始的财年内的中期期间则允许提前采纳。我们将在2024年12月31日结束的年度期间及此后的中期期间采纳这项指导。首席执行官是我们的首席经营决策者,我们将我们的经营和管理业务视为一个经营部门。
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2. 特定资产负债表项目的组成
库存
2020年9月30日
2024
12月31日
2023
 (以千为单位)
进行中的工作7,764 8,233 
成品8,050 7,741 
19,78215,814 15,974 
少量战略库存分类为非流动资产(7,764)(8,244)
总库存被归类为流动资产$8,050 $7,730 
我们依靠 制造商为我们的药物生产活性药物成分(“API”)。我们已经购买并持有大量的 API,包括在建库存中。我们将预计在资产负债表之日起 12 个月内不会出售的库存归类为 “战略库存”,即非流动资产。
预付费用和其他流动资产
2020年9月30日
2024
12月31日
2023
(以千为单位)
预付费用$5,817 $4,319 
延期处理临床资料5,707 13,496 
临床存款2,771 3,865 
其他资产4,580 5,882 
预付款和其他流动资产总计$18,875 $27,562 
应计负债及其他负债
2020年9月30日
2024
12月31日
2023
 (以千为单位)
政府返利$38,799 $18,468 
应计的薪资27,568 25,457 
已计销售与营销成本3,959 1,771 
法律费用1,836 542 
其他7,302 5,390 
已计应付及其他负债总额$79,464 $51,628 
其他
截至2024年9月30日和2023年12月31日,其他资产包括$6.0万美元和6.4 用于临床试验的存款分别为百万美元。
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3. 可供出售金融资产和公允价值衡量
我们的简明综合资产负债表中可供出售证券如下:
2020年9月30日
2024
12月31日
2023
(以千为单位)
现金等价物$110,789 $97,170 
短期市场证券243,047 232,670 
长期有价证券167,310 57,176 
总计可出售证券$521,146 $387,016 
以下表格按资产类型分组列出了我们可供出售证券:
 公允价值
等级制度
级别
2024年9月30日2023 年 12 月 31 日
摊销成本未实现收益总额未实现亏损总额估计公允价值摊销成本未实现收益总额未实现亏损总额估计公允价值
  (以千计)
公司债券第 2 级$300,504 $836 $(87)$301,253 $120,508 $307 $ $120,815 
商业票据第 2 级4,875 12  4,887 75,308 20 (9)75,319 
美国国债第 1 级104,171 46  104,217 93,655 61 (4)93,712 
货币市场基金第 1 级110,789   110,789 97,170   97,170 
有价证券总额$520,339 $894 $(87)$521,146 $386,641 $388 $(13)$387,016 
我们根据来自商业定价服务的报价市场价格,估计将被分类为1级的有市场价值的证券的公允价值;我们使用可能包括基准收益率、报告的交易、经纪商/交易商报价和发行人利差的输入,估计将被分类为2级的有市场价值的证券的公允价值。
我们定期审查我们的债务安防-半导体,以确定是否有任何投资由于发行人的信用不良或其他原因而受损。如果我们的投资的公允价值低于其摊销成本,我们将评估定量和主观因素-包括但不限于安全性质、信用评级变化和关于安全性发行人和行业的分析师报告、利率波动和一般市场情况-以确定是否需要对信用损失提取拨备。
我们的所有投资,包括未实现损失的投资,均未受损。投资的未实现损失是由于利率波动引起的。我们不打算卖出当前存在未实现损失的投资,并且在其摊销成本基础得到收回之前,我们几乎不太可能出售任何投资,这可能发生在其到期后。因此,我们未为这些投资录入信用减值准备。
我们将市场证券的应计利息分类为资产2.9万美元和1.7 million在2024年9月30日和2023年12月31日分别被确认为预付款和其他流动资产,记录在我们的简明合并资产负债表中。
截至2024年9月30日,我们所有的长期可流通证券的原始到期日不超过 26 个月,所有分类为短期的可流通证券的到期日均低于 一年。我们短期和长期可流通证券的加权平均到期日为 十个月 。截至2024年9月30日,我们的长期可流通证券剩余到期日介于 13在我们的年报(Form 10-K)中描述的合同协议方面,没有实质性的变化。24 个月之间。截至2024年9月30日,我们的可流通证券在过去3个月和9个月内没有从一个公平值分层转换为另一个。
4. 承诺和事后约定
在截至2023年12月31日的年度10-k报告中描述的合同协议下,我们的义务没有发生实质性变化。
在业务的正常过程中,我们可能会面临法律诉讼和监管行动,这可能会对我们的业务或财务状况产生重大不利影响。我们通过分析潜在的情况来评估在此类情况下的潜在责任
12

在各种诉讼、监管和和解策略下的结果。如果我们判断可能会发生损失,并且可以合理估计损失金额,我们会计提相应金额等于估计损失金额。
Melucci诉讼和解决方案
2019年3月14日,尼古拉斯·梅鲁奇(Nicholas Melucci)向美国加利福尼亚北区地方法院提起了所谓的证券集体诉讼(Melucci 诉 Corcept Therapeutics Incorporated 等,第 5:19 号案例-cv-01372-LHK)(“梅鲁奇诉讼”)。该投诉将我们和我们的某些执行官列为被告,指控他们违反了《交易法》第10(b)和20(a)条以及根据该法颁布的第100亿条第5条,并指控被告作出了虚假和具有重大误导性的陈述,没有披露有关我们业务、运营和前景的负面事实。该投诉称,假定集体诉讼期从2017年8月2日延长至2019年2月5日,并要求提供未指明的金钱救济、利息和律师费。2019年10月7日,法院任命了首席原告和首席律师。首席原告的合并申诉于2019年12月6日提出。
2023年2月8日,我们原则上达成了一项协议(“拟议和解”)以解决Melucci诉讼中的所有索赔。如先前披露的,我们根据拟议和解支付了一次性款项$14.0百万至第三方托管账户,该款项为拟议和解所要求,我们的保险公司后来已全额退还了我们这笔款项。2024年6月6日,美国加利福尼亚北部地区联邦地方法院法官James Donato批准了拟议和解的最终认可,该和解将管理向原告类成员支付的款项。
损失和 迄今已记录为损失准备金。有关我们正在进行的法律事项的进一步信息,请参阅 第二部分第1项,法律诉讼。
5. 租约
2024 年 4 月,我们签订了 六年 向Zuora, Inc.转租(“转租”),用于位于加利福尼亚州雷德伍德城红木海岸公园大道101号的办公空间,自2024年7月1日起生效。租赁的物业成为我们的新总部,自 2024 年 8 月 1 日起生效。受转租约约束的房屋部分是 50,632 可出租的平方英尺。由于拥有抢先体验权,转租于2024年6月1日开始,并将于2030年6月30日结束。我们有义务支付平均$的基本租金1.5在租赁期内每年一百万美元。根据该协议,我们根据未来租赁付款的现值记录了与租赁财产相关的使用权资产和相应的租赁负债。
我们在加利福尼亚Menlo Park的前总部租约于2024年8月31日到期。对于租期在12个月及以下的租赁,我们不承认使用权资产或租赁负债,而是按照直线法在租赁期内在简明综合收入表中确认相关的租赁付款。因此,由于剩余租期不足12个月,我们没有记录与我们的前总部相关的额外使用权资产和相应的租赁负债。
由于我们的设施经营租赁合同未提供足够的信息来确定隐含借贷利率,我们使用折现率计算了剩余租赁支付的现值,折现率等于我们支付具有月度支付和期限等于月度支付和剩余租期的抵押贷款上的利率。经营租赁使用权资产还包括在开始日期之前支付的任何租金,扣减任何获得的租赁激励。我们使用直线法在租赁期内识别经营租赁支付为费用。
2024年9月30日结束的三个月和九个月的经营租赁费用分别为$0.7万美元和2.1万美元,较上年同期的0.6万美元和1.8 百万美元,在2023年相应时期内。
与经营租赁相关的补充信息如下(单位:千美元,除加权平均数外):
截至9月30日的三个月,截至9月30日的九个月
2024202320242023
经营租赁负债的现金支付$ $617 $1,358 $1,774 
认可权益资产以交换租赁责任$ $297 $5,745 $297 
加权平均剩余租赁期限696个月96个月
加权平均折扣率8.5 %8.0 %
截至2024年9月30日,非可取消的资本化经营租赁的未来最低租赁付款如下(以千为单位):
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2024(余数)$ 
20251,382 
20261,551 
20271,598 
20281,646 
此后2,555 
减:表示利息的金额8,732 
减去隐含利息(1,941)
营业租赁负债现值$6,791 
6. 股东权益
库存股
2024年1月,我们的董事会批准了一个计划,授权回购高达$的普通股。200 该计划授权的回购金额可在公开市场、私下协商的交易或其他形式中进行。任何回购的时间和金额将根据市场条件、我们的股价和其他因素确定。该计划不要求我们回购任何特定数量的股份,并且可以根据需要随时修改、暂停或终止,无需事先通知。
在截至2024年9月30日的三个月和九个月内,我们购买了 0.30.5万股普通股,在股票回购计划下通过公开市场交易平均价格为$34.02 和 $32.25 每股,分别为购买总价$11.7万美元和15.7 万股普通股。截至2024年9月30日,尚有授权可用于回购我们的普通股。184.3 万美元。
我们按成本在我们的简明综合资产负债表上记录已购股票。截至2024年9月30日和2023年12月31日,我们持有 32.430.9百万股库存股。
激励计划
我们有之一 股权奖励计划 - corcept医疗公司2024激励奖励计划(“2024计划”)。
2024年2月,我们的董事会批准了2024年计划,在2024年5月17日举行的股东年会上获得股东批准后生效,并取代了corcept医疗公司的2012年激励奖励计划(“2012计划”)。根据2024年计划授予或转让的奖励所涉及的股份总数等于(i)xxx百万股,(ii)xxx百万股,这等于2024年5月17日2012计划下未来授予的股份数量,以及(iii)2012计划下未来授予的任何奖励,截至2024年5月17日或之后因任何原因而终止,到期或失效而未向持有人交付股份。 2024年5月17日后,将不再根据2012计划发放任何额外奖励。 8.0百万股, 4.1百万股,这等于2024年5月17日2012计划下未来授予的股份数量,以及2012计划下未来授予的任何奖励,在2024年5月17日或之后终止、到期或失效而未向持有人交付股份。2024年5月17日后,将不再根据2012计划发放任何额外奖励。
根据2024年计划,我们可以向员工、高管、董事和顾问发行股票期权、股票购买权、股票增值权和限制性股票奖励。
股票期权
截至2024年9月30日止的三个月和九个月内,我们发行了 1.01.8 百万股普通股,对应行使期权。部分期权持有人按“净行使”方式行使其期权,根据该方式,他们向我们交出,我们按当时市价从他们那里购买,价值等于相关行使价格和税款扣除义务的股票。截至2024年9月30日止的三个月和九个月内,我们分别购买了 0.50.8百万股股票,用于此类期权净行使,并支付了10.5万美元和12.2百万美元,分别用于支付相关税款扣除义务。
在截至2023年9月30日的三个月和九个月期间,我们发行了 1.02.0各自发行了百万股普通股进行期权行使。一些期权持有人以“净行使”方式行使了他们的期权,根据该方式,他们向我们交出,并且我们按当时的市场价格从他们购买了价值等同于相关行使价格和税金代扣义务的股份。截至2023年9月30日的三个月和九个月期间,我们
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购买0.61.1分别交易了200万股、500万股的期权及支付了$4.21百万美元和6.8分别支付了1000万美元以满足相关的税款代扣义务。
限制性股票奖励(“RSA”)
截至2024年9月30日的三个月和九个月,我们向员工授予了 0.20.8百万限制性股票奖励,加权平均授予日公允价值为$34.58 和 $27.07 每股的分享,分别。截至2023年9月30日的三个月和九个月,我们向员工授予了 0.10.5百万限制性股票奖励,加权平均授予日公平价值为$26.96 和 $23.26 每股应享有的投票以及分红权责。因此,RSAs被视为“享有权”股份,用于计算基本和摊薄每股净利润。请参阅下文中的“第7条注释”。
员工股票购买计划(“ESPP”)
我们的 ESPP 允许员工通过工资扣除的方式预留最多 他们购买我们普通股的年度薪酬的百分比。股票于3月1日、6月1日、9月1日和12月1日(或者,如果这些日期是节假日或周末,则在之后的第一个工作日)向2024年计划的参与员工发行,按当时交易收盘时确定的我们股票当时的公允市场价值。
对于每一股购买的股票,参与员工将获得一股配套股票,如果符合特定条件,则还可以从2024年计划中发行。根据ESPP购买而发行的股份无需归属要求。配套股票将以RSA形式授予,将在对应ESPP购买日期的周年纪念日上归属,净扣除适用的税款。 一年 RSA的归属条件是参与员工需持有自ESPP购买日起的若干年的相应股票。根据ESPP购买的股票和任何配套股票可以由员工自行保留、出售或转让。 一年 根据ESPP购买的股份和任何配套股票可以由员工全权决定保留、出售或转让。
截至2024年9月30日和2023年12月31日,我们在未经审计的简明综合资产负债表中的"应计及其他负债"项下,分别负有$2.7万美元和2.3 百万美元的以RSAs形式授予的股权补偿相关的责任。
2021年6月,公司采用了2021年员工、董事和顾问股权激励计划(“2021计划”),并进行了修改,授权公司授予最多83,564股普通股。2022年,公司修改了2021计划,并将计划授权的股票总数增加至2,748,818股。2024年1月,公司采用了2024年员工、董事和顾问股权激励计划(“2024计划”),授权公司授予最多3,900,000股普通股,加上2021计划中剩余的未授予或被放弃的股票。截至2024年3月31日,还有3,939,333股可供授予。公司的股票期权根据授予协议中的条款授予,通常按比例赠与。
以下表格总结了我们按账户分类的股权报酬情况:
截至9月30日的三个月截至9月30日的九个月
 2024202320242023
 (以千计)
资本化股票薪酬$95 $44 $223 $170 
销售成本24 11 49 43 
研究和开发4,660 4,023 13,018 11,169 
销售、一般和管理11,418 8,841 31,491 24,663 
股票薪酬总额$16,197 $12,919 $44,781 $36,045 
7. 每股净收益
我们按照参与股份的公司所需的两类股本计算基本和摊薄每股净利润。 根据两类股本法,净利润通过将净利润分配给普通股和未获授予的RSA之间来确定。 我们通过将归属于普通股股东的净利润除以期间内流通的平均普通股数量来计算基本每股净利润。 我们通过将归属于普通股股东的净利润除以期间内流通的平均普通股数量来计算摊薄每股净利润,包括可能具有摊薄效应的股票期权和未获授予的受限制股票单位(“RSU”),减去未获授予的RSA。 我们使用库存法来确定由股票期权和未获授予的RSU导致的普通股摊薄股数。
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以下表格显示了每个时期每股净利润的计算:
截至9月30日的三个月截至9月30日的九个月
 2024202320242023
 (以千为单位,每股金额除外)
分子:  
归属于普通股股东的净收益$46,690 $31,172 $109,344 $74,353 
分母:
用于计算普通每股净利润的加权平均份额103,371 102,014 103,094 103,933 
员工期权和未授予RSU的摊薄效应10,352 9,085 8,477 8,121 
用于计算每股稀释净利润的加权平均股份113,723 111,099 111,571 112,054 
每股基本净利润$0.45 $0.31 $1.06 $0.72 
每股稀释净利润$0.41 $0.28 $0.98 $0.66 
截至2024年9月30日,我们拥有 25.0 百万股票期权, 1.2 百万限制性股票奖励, 0.1 百万限制性股票单位待发放。截至2023年9月30日,我们持有 23.3 百万股票期权, 0.7 百万限制性股票奖励, 0.1 百万限制性股票单位待发放。
在加权平均基础上排除了在2024年9月30日结束的三个月和九个月中的未行使的百万股期权,以计算稀释每股净利润。1.0500万股,并且总成本(包括佣金和消费税)分别为$8.6 分别在截至2024年9月30日的三个月和九个月以及截至2023年9月30日的三个月和九个月中,我们排除了未行使的百万股期权,因为包含它们会降低稀释效果。 6.3500万股,并且总成本(包括佣金和消费税)分别为$9.0 分别在截至2023年9月30日的三个月和九个月中,我们排除了未行使的百万股期权,因为包含它们会降低稀释效果。
8. 所得税
2024 年6月30日和2023 年6月30日的期权式股票竞争行权单元的加权平均授予日期公允价值分别为 $10。5.7万美元和19.1 2024年9月30日结束的三个月和九个月分别为美元的所得税费用,相比之下,2019年12月31日结束的三个月和九个月的所得税费用为美元。5.0万美元和13.0 2019年12月31日结束的三个月和九个月的所得税费用分别为美元,与2023年相应期间相比,2024年9月30日结束的三个月和九个月的增加主要是由于税前账面收入增加。
我们的有效税率与联邦法定税率不同,这是因为州所得税以及我们股权补偿中不可抵扣部分的存在,导致我们的税收支出增加,但又被研发积分和员工期权行使所得的超额税收减免抵消,从而减少我们的应税收入。
截至2024年9月30日止三个月和九个月,未确认的税务优惠增加了$1.3万美元和3.42024年4月30日和2023年4月30日的六个月内的外汇重新计量净收益分别为$百万。
每个季度我们评估我们将产生足够应税所得以使用联邦和州递延税款资产的可能性。除了抵销我们加利福尼亚州净递延税款资产价值的减值准备金之外,我们已经确定我们很可能会实现与所有其他递延税款资产相关的利益。在我们增加减值准备金的范围内,我们将在做出这种决定的期间在简明综合收入表中包括一项费用。
自2022年开始,2017年的税收削减和就业法案取消了抵扣研发支出的权利,而是要求所有美国和外国的研发支出分别在五年和十五年的税务年限内摊销。国会曾考虑过推迟摊销要求至以后年份的立法,但截至2024年9月30日,该要求尚未修改。
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项目2.财务状况和经营成果的管理讨论与分析
下文经营管理讨论和基本报表条件及业绩分析(“MD&A”)旨在帮助读者了解我们的业务运营结果和财务状况,并作为我们简明的合并财务基本报表、基本报表附注、风险因素和其他披露的补充,请与本10-Q表格中包括的内容一起阅读。我们的简明合并财务基本报表已按照美国通用会计准则(“U.S. GAAP”)编制。
我们在本节中做出的声明属于联邦证券法的“前瞻性声明”。要全面讨论这些声明以及可能影响其准确性的潜在风险和不确定性,请参阅本10-Q表格的“风险因素”部分以及本MD&A的“概述”和“流动性和资本资源”部分。
概述
我们是一家商业阶段公司,致力于发现和开发药物,用于治疗严重的内分泌、肿瘤、代谢和神经疾病,通过调节激素皮质醇的作用。自2012年以来,我们推出了Korlym®,用于治疗患有库欣综合症的患者。在2024年6月,我们推出了Korlym的授权仿制药版本,用于相同适应症。我们的专有选择性皮质醇调节剂组合包括四个在结构上不同的系列,总共超过1,000种化合物。
库欣综合征
Korlym。 我们在美国销售Korlym和一个Korlym的仿制版本,利用销售代表拜访为患有高皮质醇症(库欣氏综合征)的患者提供照护的医生。我们还有一支基于现场的医学科学联络官队伍。我们利用专业药房和专业经销商分发我们的药物,并为医生和患者提供后勤支持。我们的政策是,不会因为财务原因而拒绝为有库欣氏综合征的患者提供我们的药物。为了帮助我们实现这一目标,我们设立了患者支持计划,并向独立的慈善基金会捐款,帮助患者支付库欣氏综合征治疗的所有方面,无论是否包括服用我们的药物。
由于大多数患有库欣综合症的人未经正确诊断或治疗,我们制定并不断完善和扩展计划,旨在教育医生和患者进行高皮质醇血症筛查,并介绍 Korlym 在治疗患有该疾病的患者中的作用。我们正在进行一项研究(“CATALYST”),旨在判断患有难以控制的糖尿病(即 HbA1c 高于7.5%)的患者中库欣综合症的患病率。在首阶段的 CATALYST 中,共有1,055名患者入组,其中发现24%的患者患有高皮质醇血症。这些患者有机会参加 CATALYST 的第二阶段,符合条件的患者将以2:1的比例随机分配接受 Korlym 或安慰剂治疗24周。我们期望来自 CATALYST 的患病率和治疗数据能帮助医生更好地识别患有库欣综合症的患者,并确定他们的最佳治疗方案。
Relacorilant。 我们正在开发我们专有的、选择性的皮质醇调节剂Relacorilant,作为库欣氏综合症患者的治疗。 Relacorilant与Korlym对糖皮质激素受体(GR)的亲和性相似,但与Korlym不同,不具有孕激素受体(PR)的亲和性,因此不是“流产药丸”,也不会引起与PR亲和性有关的其他效应,包括子宫内膜增厚和阴道出血。由于Relacorilant也不会显著增加皮质醇水平,因此不会导致低钾血症(低钾),这是患者停止使用Korlym治疗的主要原因之一。Korlym的关键试验中,44%的患者出现低钾血症。与用于治疗库欣氏综合症的所有其他药物不同,Relacorilant不会延长心脏的QT间期,这是一种可能致命的非靶效应。
我们已经完成了relacorilant在Cushing综合症患者中的两项3期试验-我们的关键试验“GRACE”和我们的“GRADIENT”试验。在这两项试验中,患者表现出高血压、血糖控制、体重和体成分以及其他Cushing综合症体征和症状方面具有临床意义的改善。Relacorilant的耐受性良好。值得注意的是,患者没有经历Korlym或其他目前批准治疗中可能出现的一些严重不良事件。
GRACE试验分为两部分。首先是开放标签阶段,招募了152名任何患有库欣氏综合征病因的患者。每位患者接受relacorilant治疗22周。表现出预先规定改善的高血压、高血糖或两种症状中任何一种的患者,继续进行GRACE的第二个,双盲,随机撤回阶段,其中一半的患者继续接受relacorilant,另一半接受安慰剂治疗12周。GRACE的主要终点是继续接受relacorilant治疗的患者失去血压控制,与将relacorilant替换为安慰剂的患者进行比较。
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在开放标签阶段,患者在广泛的库欣综合征体征和症状方面经历了临床意义和统计学显著的改善,包括高血压、高血糖、体重、腰围、脂肪和瘦体重、认知和库欣生活质量评分。
所有高血压患者的收缩压(SBP)和舒张压(DBP)均有快速且持续的改善,22周时平均SBP改善了7.9毫米汞柱,平均DBP改善了5.4毫米汞柱(p值:<0.0001)。在开放标签阶段,63%的高血压患者符合研究的响应标准。进入随机退出阶段的患者中,高血压症状的改善甚至更为显著,22周时平均SBP改善了12.6毫米汞柱,平均DBP改善了8.3毫米汞柱(p值:<0.0001)。为确保准确性,高血压是通过24小时动态血压监测(ABPM)来测量的。
葡萄糖代谢通过多个诊断测试进行测量,包括口服葡萄糖耐量试验(葡萄糖曲线下面积或AUC葡萄糖),糖化血红蛋白(HbA1c)和空腹血糖。对于所有患有糖尿病和受损葡萄糖耐量(即糖尿病前期)的患者,葡萄糖代谢均有临床意义和统计显著改善。数据显示22周时AUC葡萄糖均值改善了3.3 h*mmol/L,HbA1c均值改善了0.3%,空腹血糖均值改善了12.4 mg/dL(分别为p值:<0.0001,0.03,0.03)。在开放标签阶段,50%的高血糖患者符合研究的反应标准。进入随机撤退阶段的患者,高血糖的改善更为显著,22周时AUC葡萄糖均值改善了6.2 h*mmol/L,HbA1c均值改善了0.7%,空腹血糖均值改善了25.2 mg/dL(分别为p值:<0.0001,<0.0001,0.006)。
格雷斯在随机撤回阶段达到了血压控制丧失的主要终点,与被转换到安慰剂的患者相比,继续接受雷拉考瑞的患者的结果(比值比:0.17;p值:0.02)。继续接受雷拉考瑞的患者也保持了他们在高血糖、腰围和脂肪和瘦体重方面的改善。接受安慰剂的患者经历了肾上腺皮质功能亢进综合征体征和症状的明显恶化。
我们的第3阶段GRADIENt研究支持GRACE试验,进一步证明了relacorilant的有效性和安全性。GRADIENt研究了由肾上腺腺瘤或肾上腺增生引起的库欣综合症患者。这些患者通常表现出较轻的症状,并且比其他库欣综合症病因的患者有更渐进的下降,尽管他们的健康结局最终是糟糕的。GRADIENt招募了137名患有库欣综合症且患有高血压、高血糖或两者的患者。患者以双盲方式以1:1随机分配,分别接受relacorilant或安慰剂治疗22周。试验的主要终点是与安慰剂相比改善收缩压并控制血糖,体重和体脂含量作为次要终点。
在接受relacorilant治疗的GRADIENt患者中,与基线相比,高血压、高血糖、体重和体成分方面表现出临床意义和统计学上显著的改善,而接受安慰剂治疗的患者则没有。
接受relacorilant治疗的高血压患者,平均收缩压下降了6.6毫米汞柱(p值0.012),与基线相比。接受安慰剂的患者收缩压下降了2.1毫米汞柱(p值:ns),与基线相比。接受relacorilant和安慰剂的患者之间的比较在统计学上没有显著差异。在研究期间,5名接受安慰剂治疗的患者需要抗高血压药物的抢救治疗,而只有1名接受relacorilant治疗的患者需要。为确保准确性,高血压是通过24小时动态监测血压来测量的。
接受relacorilant治疗的高血糖患者在葡萄糖代谢方面经历了临床意义重大且统计学上显著的改善,包括空腹血糖(与安慰剂相比减少了22.2 mg/dL;p值0.002)、口服葡萄糖耐量试验下曲线面积(与安慰剂相比减少了2.6 h*mmol/L;p值0.046)和A1c血红蛋白(与安慰剂相比减少了0.3个百分点;p值0.019)。
在GRADIENt接受relacorilant治疗的患者,体重和内脏脂肪质量和成交量均显著改善(相比接受安慰剂的患者,体重减轻了3.9公斤,p值为0.0001;内脏脂肪质量和成交量的p值分别为0.018和0.016)。
Relacorilant在GRADIENt中耐受性良好,副作用与其在第2期和GRACE试验中观察到的一致。在所有这些研究中,最常见的不良事件包括轻至中度恶心、水肿、四肢和背部疼痛以及疲劳 - 所有这些症状都与很多患者在手术后或开始治疗库欣氏综合征的过程中经历的“皮质醇戒断”有关。重要的是,在这些实例中没有出现由relacorilant引起的低钾血症、子宫内膜增生或相关的阴道出血、肾上腺功能不全或QT间期延长。
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美国食品药品监督管理局(“FDA”)和欧盟委员会(“EC”)已将relacorilant指定为库欣征兆的孤儿药物。在美国,relacorilant的孤儿药物指定将获得税收抵免、减少监管费用,并且如果我们获得库欣征兆治疗的批准,将获得七年的独家营销权利。欧盟的孤儿药物指定也带来类似的好处,但还包括欧洲药品管理局(“EMA”)的协议援助、在欧盟获得专门营销授权程序的准入,以及如果我们获得批准,将获得在欧盟为库欣征兆患者治疗的十年独家营销权利。
肿瘤学
有充分证据表明,在某些抗癌疗法中,皮质醇在G蛋白偶联受体上的活性会降低效力,并且调节皮质醇的活性可能有助于抗癌治疗实现预期效果。在某些癌症中,皮质醇抑制细胞凋亡 - 很多治疗方案旨在刺激的杀伤肿瘤效应。而在其他癌症中,皮质醇的活性促进肿瘤生长。皮质醇还会抑制人体的免疫反应;激活 - 而不是抑制 - 免疫系统有助于对抗某些癌症。许多实体瘤表达G蛋白偶联受体,并且是皮质醇调节疗法的潜在靶点,其中包括卵巢癌、肾上腺癌和前列腺癌。
铂金耐药性卵巢癌患者中的Relacorilant。 我们正在进行一个关键的3期试验(“ROSELLA”),使用我们的专有、选择性皮质醇调节剂Relacorilant与nab-紫杉醇联合治疗铂金耐药性卵巢癌患者。ROSELLA的入组已经结束。381名有复发性、铂金耐药性卵巢癌的妇女被随机分为1:1,分别接收间断150毫克的Relacorilant和nab-紫杉醇或者nab-紫杉醇单药治疗。ROSELLA的主要终点是无进展生存期(“PFS”),整体生存期是一个关键的次要终点。参加ROSELLA的患者需要接受过先前的Bevacizumab治疗,这是治疗铂金耐药性卵巢癌患者的已批准标准疗法。患有对最初的铂金类药物治疗无反应的肿瘤史(即患有“初次铂金耐药性”疾病的妇女)以及接受过三条以上治疗线的妇女被排除在外。
ROSELLA旨在复制我们的2期试验的积极结果,这是一项治疗铂金耐药性卵巢癌患者的178例受控多中心试验,包括relacorilant与nab-紫杉醇联合治疗。2期研究参与者被随机分配到三种治疗组中的一组:60名女性间断性地接受150毫克relacorilant(在每周接受nab-紫杉醇治疗的前一天、当天和第二天);58名女性每天额外服用100毫克的relacorilant,同时接受nab-紫杉醇治疗;60名女性仅接受nab-紫杉醇治疗。试验的主要终点是无进展生存期(PFS)。
在2期试验的relacorilant加nab-紫杉醇治疗组中,患者的无进展生存期(PFS)比单独接受nab-紫杉醇的患者更长。间歇性接受更高剂量relacorilant的患者在中位PFS上表现出明显改善(5.6个月对比3.8个月,风险比:0.66;p值:0.038)。每日接受较低剂量relacorilant的患者显示出比单独接受nab-紫杉醇的患者更长的中位PFS(5.3个月对比3.8个月,风险比:0.83;p值:无显著差异)。间歇性接受relacorilant的患者还具有比单独接受nab-紫杉醇的患者更长的反应持续时间(DoR)(5.6个月对比3.7个月,风险比:0.36;p值:0.006)。间歇性接受relacorilant的患者也活得更久(中位总生存期:13.9个月对比12.2个月,风险比:0.67;p值:0.066)。
在第2期试验中,将relacorilant添加到nab-紫杉醇治疗中,并未为患者带来额外的不良事件负担。 relacorilant加nab-紫杉醇的安全性和耐受性与nab-紫杉醇单药疗法相当。
我们第二阶段试验的最终分析已发表在 《临床肿瘤学杂志》2022年第40卷21期2321-2332页: Burtness亿.等。 《关键点048中的Pembrolizumab单药或联合化疗用于复发/转移性头颈鳞状细胞癌:通过编程死亡配体1合并阳性评分的亚组分析》。请注意,5.4%的ORR和32.4%的DCR是根据具有CPS的37位可评估患者计算得出的 (Colombo等,2023),美国临床肿瘤学会(ASCO)的重要期刊。
Relacorilant在有皮质醇过多的肾上腺癌患者中的应用。 我们已经完成了一个开放标签的Phase 10亿试验,试验中包括了14位转移性或不可切除的肾上腺癌患者,这些患者的肿瘤会产生皮质醇。患有这种形式的肾上腺癌的患者几乎不会对免疫疗法产生响应,肿瘤的进展非常迅速。我们的试验旨在检验在pembrolizumab疗法中添加relacorilant是否足以减少皮质醇激活的免疫抑制,以帮助患者的免疫系统减少或清除患者的肿瘤,同时减轻肿瘤过度产生皮质醇引起的库欣氏综合征症状。 虽然我们试验中的患者症状,如高血压和高血糖,有显著改善,但肿瘤的进展并没有放缓。relacorilant与pembrolizumab的组合耐受性良好。我们正在评估下一步措施,以进一步了解皮质醇调节与免疫疗法在其他肿瘤类型和早期癌症阶段中的作用。
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前列腺癌患者中的Relacorilant去势疗法是前列腺癌的标准治疗,因为雄激素刺激前列腺肿瘤生长。皮质醇也会刺激前列腺肿瘤生长,皮质醇在糖皮质激素受体处的作用可能导致肿瘤逃脱雄激素剥夺疗法。将皮质醇调节剂与雄激素调节剂结合可能阻断这一逃逸路径。我们在芝加哥大学的合作伙伴已经开始了在前列腺癌患者,术前的前列腺切除患者中对Relacorilant和Enzalutamide进行随机、安慰剂对照的2期试验。我们为研究提供了Relacorilant和安慰剂。 我们从芝加哥大学获得的专利涵盖了使用Relacorilant与抗癌药物,包括Enzalutamide,用于治疗具有这一适应症的患者。
肌萎缩侧索硬化(“ALS”)
ALS,又称为路易·格里格病,是一种毁灭性的神经肌肉疾病。我们的选择性皮质醇调节剂达祖考利昔在ALS动物模型中改善了运动表现,并减少了神经炎症和肌肉萎缩。在这些令人信服的结果之后,我们启动了达祖考利昔在ALS患者中的2期试验(“DAZALS”)。249名患者进行了随机分组,以双盲方式1:1:1接受每天150毫克达祖考利昔、300毫克达祖考利昔或安慰剂治疗24周。DAZALS的主要终点是ALS功能评定量表-修订版(ALSFRS-R)在接受达祖考利昔和接受安慰剂治疗的患者之间的差异。招募工作已完成。FDA已将达祖考利昔指定为美国ALS治疗的孤儿药品。
代谢性疾病
肝病。 代脂肝疾病(MASH)是代谢紊乱相关脂肪肝病的一种爱文思控股形式,困扰着数百万患者,是与肝脏有关的死亡的主要原因。我公司爱文思控股试验阶段的选择性皮质醇调节剂米力可瑞兰作为一种治疗MASH潜在药物的试诊确定了一种剂量方案,可以减少肝脂肪,改善肝脏健康和主要代谢和脂质指标,而且耐受良好。在取得这些触目惊心的结果后,我们于2023年10月开始了随机、双盲、安慰剂对照的第20亿阶段试验(“MONARCH”),以检查米力可瑞兰在患有MASH的患者中的效果。MONARCH有两个患者队列。A队列计划招募120名经活检确认患有MASH的患者,随机分组为2:1,分别接受每周两次100毫克的米力可瑞兰或安慰剂治疗48周。A队列的主要终点是减少肝脂肪,而MASH缓解和纤维化改善为关键次要终点。B队列计划招募75名被推断为患有MASH的患者,随机分组为2:1,分别接受每周两次100毫克的米力可瑞兰治疗6周,然后每周两次200毫克的米力可瑞兰治疗18周,或安慰剂治疗24周。B队列的主要终点是减少肝脂肪。
抗精神病药物引起的体重增加(“AIWG”). 在美国,有600万人正在服用抗精神病药物,如奥氮平和利培酮,用来治疗精神分裂症、躁郁症和抑郁症等疾病。虽然这些药物非常有效,但它们常常会引起迅速和持续的体重增加,其他代谢紊乱,最终甚至导致心血管疾病。我们在服用抗精神病药物后体重增加的患者中进行了两项miricorilant的2期试验。然而,在这些研究中,接受miricorilant的患者并没有减轻体重。2023年10月,我们开始了一项第1期试验,研究miricorilant预防AIWG的潜力,但由于缺乏功效,我们于2024年6月终止了该试验。
药物发现和临床前开发
我们继续从我们的选择性皮质醇调节剂组合中鉴定新化合物,并推进其中最有前景的化合物进入临床阶段。
2022年通胀缩减法
2022年8月16日,通货膨胀减缓法案(IRA)被颁布。IRA包括规定,如果Medicare b部分或D部分药品的价格上涨速度超过通货膨胀率,制造商需要向医疗保险与医疗补助中心(CMS)支付回扣。此外,从2025年开始,IRA还将把目前由政府和受益人分担的医疗保险受益人成本的重要部分转移到制造商身上。我们预计这一规定将极大限制我们从Medicare患者处获得的营业收入,并可能在很大程度上减少我们的利润。IRA允许CMS就某些高支出的Medicare b部分或D部分药品进行价格谈判。
IRA还对某些股票回购征收1%的消费税,并对调整后的基本报表收入引入15%的企业备选最低税。企业备选最低税于2024年1月1日对我们生效。我们不预计这两项规定会对我们的综合财务报表产生重大影响。
请查看本季度10-Q表格中第1A条款下的风险因素。 新的法律、政府法规或对现行法律和法规的更改可能会使我们难以获得可接受的价格或足够的
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保险覆盖和药物报销,可能对我们的运营结果和财务状况产生不利影响.”
经营结果
净产品营业收入 净产品收入是指销售给我们客户的总产品收入,扣除了预计政府折扣和退款、患者医疗费用援助项目、提供给我们专业分销商以获得及时付款的折扣以及预期退货准备金。
产品净收入分别为2024年9月30日结束的三个月和九个月的收入为18250万美元和49320万美元,而2023年同期分别为12360万美元和34700万美元。更高的销售量分别占2024年9月30日结束的三个月和九个月的增长的89.0%和78.6%,其余增长归因于 于2024年1月1日生效的价格上涨。
销售成本 销售成本包括原料药(API)、制片、包装、人员、制造费用、稳定性测试和分销成本。
销售成本分别为2024年9月30日结束的三个月和九个月分别为290万和790万美元,而在2023年相应期间分别为160万和460万美元。销售成本与营业收入的比例分别为2024年9月30日结束的三个月和九个月均为1.6%,而在2023年相应期间则均为1.3%。这些增加主要是由于制造业、运输和分销成本的增加。
研发费用研发费用包括(1)临床试验的费用,(2)招募和补偿开发人员的费用,(3)制造研究性药物产品的费用,(4)临床前研究的费用,(5)药物发现研究的费用和(6)新药剂型和制造工艺的研发费用。
截至2024年9月30日的三个月和九个月,研发费用分别为5930万美元和17660万美元,而2023年同期分别为4550万美元和12960万美元。这些增加是因为在推进和完成我们的开发项目以及增加员工薪酬方面的支出增加。
截至9月30日的三个月截至9月30日的九个月
 2024202320242023
(以千为单位)
临床开发计划:  
肿瘤学$13,007 $11,493 $42,237 $27,925 
库欣综合症14,273 8,980 39,930 27,747 
代谢性疾病10,406 8,122 29,914 24,597 
临床前和早期选择性皮质醇调节剂9,583 7,871 30,028 23,594 
未分配的活动,包括制造业-半导体和监管活动7,407 5,028 21,460 14,614 
以股票为基础的报酬计划4,660 4,023 13,018 11,169 
总研发费用$59,336 $45,517 $176,587 $129,646 
预测开发活动的时间和费用是困难的,存在许多不确定性和风险,包括结论不明确或为负面结果、患者入组缓慢、不良副作用以及研究药物的配方或制造困难和候选药物功效不足。此外,临床开发受到政府监督和可能会在未经通知的情况下改变的法规约束。随着我们的临床项目推进,我们预计2024年的研发支出将高于2023年。未来几年的研发支出将取决于我们的临床试验和开发计划的结果。
销售、一般和行政费用 销售、一般和行政费用包括(1)从事商务和行政活动的雇员、顾问和承包商的薪酬,(2)支持商务活动的供应商成本和(3)法律和会计费用。
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Selling, general and administrative expense was $73.7 million and $196.9 million for the three and nine months ended September 30, 2024, respectively, compared to $45.3 million and $137.1 million for the comparable periods in 2023. The increases were primarily due to increased employee compensation expenses and sales and marketing activities.
We expect our selling, general and administrative expense to be higher in 2024 than in 2023 due to increased commercial and administrative activities, including litigation and administrative support for increased research and development and marketing efforts.
Interest and other income - Interest and other income was $6.3 million and $17.8 million for the three and nine months ended September 30, 2024, respectively, compared to $5.2 million and $12.1 million for the comparable periods in 2023. The increases were due to higher cash and investment balances and market-wide increases in interest rates.
Income tax expense - Income tax expense was $5.7 million and $19.1 million for the three and nine months ended September 30, 2024, respectively, compared to income tax expense of $5.0 million and $13.0 million for the comparable periods in 2023. The increases were primarily due to increased pretax book income.
Liquidity and Capital Resources
We rely on revenues from the sale of our medications to fund our operations.
Based on our current plans and expectations, we expect to fund our operations and planned research and development activities over the next 12 months and beyond without needing to raise additional funds, although we may choose to raise additional funds for other reasons. If we were to raise funds, equity financing would be dilutive, debt financing could involve restrictive covenants and funds raised through collaborations with other companies may require us to relinquish certain rights in our product candidates.
As of September 30, 2024, we had cash, cash equivalents and marketable securities of $547.6 million, consisting of cash and cash equivalents of $137.3 million and marketable securities of $410.4 million, compared to cash, cash equivalents and marketable securities of $425.4 million, consisting of cash and cash equivalents of $135.6 million and marketable securities of $289.8 million as of December 31, 2023.
The cash in our bank accounts and our marketable securities could be reduced or our access to them restricted if the financial institutions holding them were to fail or severely adverse conditions were to arise in the markets for public or private debt securities. We have never experienced a material lack of access to cash or material realized losses.
Net cash provided by operating activities was $138.8 million for the nine months ended September 30, 2024, compared to $121.2 million for the comparable period in 2023. The increase was primarily due to higher revenue.
Net cash used in investing activities was $113.2 million for the nine months ended September 30, 2024, compared to net cash provided by investing activities of $73.8 million for the comparable period in 2023. The change was primarily due to allocation of cash proceeds from maturities of marketable securities towards cash equivalents in anticipation of the closing of our tender offer during the comparable period in 2023.
Net cash used in financing activities was $23.8 million for the nine months ended September 30, 2024, compared to $149.5 million for the comparable period in 2023. In the nine months ended September 30, 2024, we spent $31.0 million acquiring shares of our common stock, comprised of $15.7 million pursuant to our Stock Repurchase Program, $12.2 million acquiring shares of our common stock in connection with the net exercise of employee and director stock options, and $3.1 million to satisfy tax withholding requirements from vesting of restricted stock grants, offset by $3.9 million received in connection with our ESPP and $3.3 million net cash received from the exercise of stock options. In the comparable period in 2023, we spent $153.5 million acquiring shares of our common stock, comprised of $145.4 million pursuant to our tender offer, $6.8 million acquiring shares of our common stock in connection with the net exercise of employee and director stock options and $1.3 million to satisfy tax withholding requirements from vesting of restricted stock grants, offset by $3.0 million received in connection with our ESPP and $1.1 million net cash received from the exercise of stock options.
As of September 30, 2024, we had retained earnings of $513.0 million.
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Contractual Obligations and Commitments
Our contractual payment obligations and purchase commitments are disclosed in our Annual Report on Form 10-K for the year ended December 31, 2023. Other than future minimum lease payments with respect to our sublease for office space with Zuora, our payment obligations and purchase commitments did not change materially during the nine months ended September 30, 2024. See Notes 4 and 5 to our Unaudited Condensed Consolidated Financial Statements for more information regarding our purchase commitments and future minimum lease payments, respectively.
Critical Accounting Policies and Estimates
Our condensed consolidated financial statements have been prepared in accordance with U.S. GAAP, which requires us to make estimates and judgments that affect the amount of assets, liabilities and expenses we report. We base our estimates on historical experience and on other assumptions we believe to be reasonable. Actual results may differ from our estimates. Our significant accounting policies are described in our Annual Report on Form 10-K for the fiscal year ended December 31, 2023. There were no changes that occurred during the fiscal quarter covered by this report that materially affected, or are reasonably likely to materially affect, our critical accounting policies and estimates.
ITEM 3.  QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
Our market risks as of September 30, 2024 are disclosed in our Annual Report on Form 10-K for the year ended December 31, 2023. The market risks associated with our cash, cash equivalents and marketable securities, which consist entirely of debt instruments with original maturities of less than 26 months did not change materially during the nine months ended September 30, 2024.
ITEM 4.  CONTROLS AND PROCEDURES
Evaluation of disclosure controls and procedures. As of September 30, 2024, our management conducted an evaluation, under the supervision and with the participation of our Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and operation of our disclosure controls and procedures, as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934 (the “Exchange Act”). Based upon that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that, as of September 30, 2024, our disclosure controls and procedures were effective to provide reasonable assurance that the information required to be disclosed by the Company in the reports that it files or submits under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in SEC rules and forms and that such information is accumulated and communicated to the officers who certify our financial reports and to the members of the Company’s senior management and board of directors as appropriate to allow timely decisions regarding required disclosure at the reasonable assurance level.
Changes in internal control over financial reporting. Our Chief Financial Officer and other members of management evaluated the changes in our internal control over financial reporting during the quarter ended September 30, 2024 and concluded that there was no change during the quarter that materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
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PART II. OTHER INFORMATION
ITEM 1.  LEGAL PROCEEDINGS
Teva Patent Litigation
In February 2018, we received a Paragraph IV Notice Letter advising that Teva Pharmaceuticals USA, Inc. (“Teva”) had submitted an Abbreviated New Drug Application (“ANDA”) to the FDA seeking authorization to manufacture and sell a generic version of Korlym prior to the expiration of patents related to Korlym that are listed in the FDA’s Approved Drug Products with Therapeutic Equivalence Evaluations (the “Orange Book”). In March 2018, we filed a lawsuit in the United States District Court for the District of New Jersey (“D.N.J.”) against Teva for infringement of our patents. In August 2020, Teva received final approval from the FDA for its ANDA in accordance with the Hatch-Waxman Act.
In May 2019, Teva submitted to the Patent Trial and Appeal Board (“PTAB”) a petition for post-grant review (“PGR”) of U.S. Patent No. 10,195,214 (the “’214 patent”). In November 2020, the PTAB issued a decision upholding the validity of the ’214 patent in its entirety, which decision the Federal Circuit Court of Appeals upheld. This matter is closed.
The patents currently at issue in the D.N.J matter are the ʼ214 patent and U.S. Patent No. 10,842,800 (the “’800 patent”). Trial was held from September 26, 2023 through September 28, 2023 before Judge Renee Marie Bumb. On December 29, 2023, Judge Bumb ruled that Teva’s proposed generic product would not infringe either the ’214 or ’800 patent. We have appealed that ruling to the United States Court of Appeals for the Federal Circuit. Teva launched its generic product in January 2024.
We will vigorously enforce our intellectual property rights relating to Korlym but cannot predict the outcome of these matters.
Teva Antitrust Litigation
On June 13, 2024, Teva filed a complaint in the Northern District of California, captioned Teva Pharmaceuticals USA, Inc. v. Corcept Therapeutics, Inc., et al. (N.D. Cal.), Case No. 3:24-cv-03567-BLF (the “Teva Antitrust Litigation”). This lawsuit names Corcept and Optime Care, Inc. (“Optime”), our single specialty pharmacy that dispenses Korlym and performs related pharmacy and patient support services, as defendants and alleges, among other things, that Corcept has violated federal and state laws related to antitrust and unfair business practices. On August 26, 2024, Corcept and Optime filed motions to dismiss the complaint. On September 13, 2024, Teva filed a First Amended Complaint, and on October 14, 2024, Corcept and Optime moved to dismiss the First Amended Complaint. A hearing on the motion to dismiss has been scheduled for February 20, 2025.
Other Litigation
In March 2019, a purported securities class action complaint was filed in the United States District Court for the Northern District of California by Nicholas Melucci (Melucci v. Corcept Therapeutics Incorporated, et al., Case No. 5:19-cv-01372-LHK) (the “Melucci litigation”). The complaint named us and certain of our executive officers as defendants asserting violations of Sections 10(b) and 20(a) of the Exchange Act and Rule 10b-5 promulgated thereunder and alleged that the defendants made false and materially misleading statements and failed to disclose adverse facts about our business, operations and prospects. The complaint asserted a putative class period extending from August 2, 2017 to February 5, 2019 and sought unspecified monetary relief, interest and attorneys’ fees. On June 6, 2024, Judge James Donato of the United States District Court for the Northern District of California granted final approval of a settlement resolving all claims in the Melucci litigation (the “Melucci Settlement”). As previously disclosed, the Melucci Settlement required us to make a one-time payment of $14 million for which our insurers reimbursed us in full. On September 6, 2024, Judge Donato approved the Plan of Allocation for payment of the settlement funds to eligible members of the class of plaintiffs. This matter is closed.
In September 2019, a purported shareholder derivative complaint was filed in the United States District Court for the District of Delaware by Lauren Williams, captioned Lauren Williams v. G. Leonard Baker, et al., Civil Action No. 1:19-cv-01830. A second nearly identical lawsuit was filed in December 2019 in the United States District Court for the District of Delaware by Jeweltex Pension Plan, captioned Jeweltex Pension Plan v. James N. Wilson, et al., Civil Action No. 1:19-cv-02308. These complaints named the then-existing members of our board of directors, our Chief Executive Officer and our current Chief Business Officer as defendants, and Corcept as a nominal defendant. The complaints allege breach of fiduciary duty, violation of Section 14(a) of the Exchange Act, insider selling, misappropriation of insider information and waste of corporate assets and seek damages in an amount to be proved at trial. These actions had been stayed pending resolution of the Melucci litigation. On June 21, 2024, the United States District Court for the District of Delaware lifted the stays on the Williams and Jeweltex cases and consolidated these two cases into one case.
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In January 2022, a purported shareholder derivative complaint was filed in the Delaware Court of Chancery by Joel B. Ritchie, captioned Joel B. Ritchie v. G. Leonard Baker, et al., Case No. 2022-0102-SG. The complaint named certain members of our Board of Directors, our Chief Executive Officer, our current Chief Business Officer and our President of Corcept Endocrinology as defendants, and Corcept as nominal defendant. The complaint alleges a single cause of action for breach of fiduciary duty. The complaint seeks damages in an amount to be proved at trial. On March 22, 2024, the Court lifted a previously-entered stay, which had been pending the resolution of the Melucci litigation, and on May 3, 2024, we filed a Motion to Dismiss this complaint. We cannot predict when the Court will rule on this motion.
Given the overlapping allegations in these shareholder derivative actions, we and the individual defendants have filed a One Forum Motion in both the United States District Court for the District of Delaware and the Delaware Court of Chancery requesting that the Courts coordinate to determine in which jurisdiction (Federal or Chancery Court) these matters should first proceed. The Courts have not yet ruled on that Motion.
We will respond vigorously to the above allegations but cannot predict the outcome of these matters.
Records Subpoena
In November 2021, we received a records subpoena from the United States Attorney’s Office for the District of New Jersey (the “NJ USAO”) pursuant to Section 248 of the Health Insurance Portability and Accountability Act of 1996 (“HIPAA”) seeking information relating to the sale and promotion of Korlym, our relationships with and payments to health care professionals who can prescribe or recommend Korlym and prior authorizations and reimbursement for Korlym. The NJ USAO has informed us that it is investigating whether any criminal or civil violations by us occurred in connection with the matters referenced in the subpoena. It has also informed us that it does not currently consider us a defendant but rather an entity whose conduct is within the scope of the government’s investigation.
In addition to the above-described matters, we are involved from time-to-time in other legal proceedings arising in the ordinary course of our business. Although the outcome of any such matters and the amount, if any, of our liability with respect to them cannot be predicted with certainty, we do not believe that they will have a material adverse effect on our business, results of operations or financial position.
ITEM 1A.  RISK FACTORS
Investing in our common stock involves significant risks. Before investing, carefully consider the risks described below and the other information in this quarterly report, including our condensed consolidated financial statements and related notes. The risks and uncertainties described below are the ones we believe may materially affect us. There may be others of which we are unaware that could materially harm our business or financial condition and cause the price of our stock to decline, in which case you could lose all or part of your investment.
Summary of Principal Risks
The following bullet points summarize the principal risks we face, each of which could adversely affect our business, operations and financial results. Below, we have arranged these risks by the part of our business they most directly affect.
Risks Related to our Commercial Activities
Failure to generate sufficient revenue from the sale of Korlym would harm our financial results and would likely cause our stock price to decline.
The availability of generic Korlym could adversely affect our business, results of operations and financial position.
Public perception of mifepristone or legislation limiting or barring its use for termination of early pregnancy may limit our ability to sell our medications.
New laws, government regulations, or changes to existing laws and regulations could make it difficult or impossible for us to obtain acceptable prices or adequate insurance coverage and reimbursement for Korlym, which would adversely affect our results of operations and financial position.
Risks Related to our Research and Development Activities
Vendors perform many of the activities necessary to carry out our clinical trials, including drug product distribution, trial management and oversight and data collection and analysis. Failure of these vendors to perform their duties or meet expected timelines may prevent or delay approval of our product candidates.
Our efforts to discover, develop and commercialize our product candidates may not succeed. Clinical drug development is lengthy, expensive and often unsuccessful. Results of early studies and trials are often not predictive of
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later trial results. Failure can occur at any time. Even if we deem that our product candidates’ clinical trial results demonstrate safety and efficacy, regulatory authorities may not agree. Failure to obtain or maintain regulatory approvals for our product candidates would prevent us from commercializing them.

Risks Relating to our Intellectual Property
To succeed, we must secure, maintain and effectively assert adequate patent protection for the composition and methods of use of our proprietary, selective cortisol modulators and for the use of Korlym to treat Cushing’s syndrome. Litigation is slow and expensive and its outcome is uncertain and subject to challenge on appeal.
Risks Related to our Stock
The price of our common stock fluctuates widely and is likely to continue to do so. Opportunities for investors to sell shares may be limited.
Our stock price may decline if our financial performance does not meet the guidance we have provided to the public, estimates published by research analysts or other investor expectations.
General Risk Factors
We rely on information technology to conduct our business. A breakdown or breach of our information technology systems or our failure to protect confidential information concerning our business, patients or employees could interrupt the operation of our business and subject us to liability.
Risk Factors – Discussion
The following section discusses the principal risks listed above, as well as other risks we believe to be material.
Risks Related to our Commercial Activities
Failure to generate sufficient revenue from the sale of Korlym would harm our financial results and would likely cause our stock price to decline.
Our ability to generate revenue and to fund our commercial operations and development programs is dependent on the sale of Korlym to treat patients with Cushing’s syndrome. Physicians will prescribe Korlym if they determine that it is preferable to other treatments, even if those treatments are not approved for Cushing’s syndrome. Most physicians are inexperienced diagnosing or caring for patients with Cushing’s syndrome and it can be hard to persuade them to identify appropriate patients and treat them with Korlym.
Many factors could limit our Korlym revenue, including:
the preference of physicians or payors for competing treatments for Cushing’s syndrome, including a lower-priced generic version of Korlym and off-label treatments; and
lack of availability of government or private insurance, the shift of a significant number of patients to Medicaid, which reimburses Korlym at a significantly lower price, or the introduction of government price controls or other price-reducing regulations, such as the Inflation Reduction Act of 2022, that may significantly limit Medicare reimbursement rates.
Failure to generate sufficient Korlym revenue could prevent us from fully funding our planned commercial and clinical activities and would likely cause our stock price to decline.
The availability of generic Korlym could adversely affect our business, results of operations and financial position.
In January 2024, Teva launched a generic version of Korlym. We have sued Teva in Federal District Court with respect to its generic version of Korlym. On December 29, 2023, the Court issued a ruling in that case finding that Teva’s generic product would not infringe the patents we have asserted against it. We have appealed this adverse decision to the Federal Circuit Court of Appeals, but there can be no assurance our appeal will be successful. If Teva’s commercial efforts are successful, they may materially harm our results of operations and financial condition, even if our appeal is successful and Teva is required to withdraw its product and pay us damages. We have made available our own generic version of Korlym.
We also have litigation settlements with Sun and Hikma that allow them to begin selling mifepristone, with customary restrictions, provided the FDA has approved their products and Teva’s generic product remains commercially available. The
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availability of generic versions of Korlym from Sun or Hikma could materially harm our results of operations and financial condition, even if our on-going appeal against Teva is successful and Teva, Sun and Hikma were required to withdraw their products and pay us damages. Please see “Part II, Item 1, Legal Proceedings” for additional details.
The availability of generic Korlym could cause our revenue to decline and materially harm our results of operations and financial position, by reducing the number of tablets we sell or lowering their price. It may also cause our revenue to be materially less than the public guidance we have provided, which would likely cause the price of our common stock to decline.
Legal action to enforce or defend intellectual property rights is complex, costly and involves significant commitments of management time. Other companies may seek FDA approval to market generic versions of Korlym, in which case we will vigorously protect our intellectual property. However, there can be no assurance our efforts will be successful.
Public perception of mifepristone or legislation limiting or barring its use for termination of early pregnancy may limit our ability to sell our medications.
The active ingredient in Korlym, mifepristone, is approved by the FDA in another drug for the termination of early pregnancy. In 2022, the United States Supreme Court published its decision in the case of Dobbs v. Jackson Women’s Health Organization (“Dobbs”), which overturned Roe v. Wade, the 1973 Supreme Court decision that had established a woman’s right to terminate her pregnancy, subject to certain limitations. Dobbs has stimulated many states to enact laws restricting the legality of abortion and mifepristone, including during early pregnancy and under specific conditions of use. More laws banning or heavily restricting termination of pregnancy may be adopted and existing laws may be made more restrictive. On June 13, 2024, in a highly publicized case, the Supreme Court ruled against plaintiffs seeking to restrict access to mifepristone for terminating pregnancy, holding that they lacked standing (i.e., the right to sue), thus preserving current access to mifepristone. Because the Supreme Court’s decision was made solely on procedural grounds, the ruling does not necessarily foreclose other challenges to the continued availability of mifepristone. The timing and outcome of any subsequent cases, as well as additional legislative changes are uncertain. In addition, heightened public awareness of mifepristone as an abortifacient may draw the attention of hostile state government officials or political activists to Korlym – as could additional public debate concerning current or proposed restrictions on the distribution of mifepristone. This may be the case even though (i) Korlym is not approved for the termination of pregnancy, (ii) we do not promote it for that use and (iii) we have taken measures to minimize the chance that it will accidentally be prescribed to a pregnant woman.
New laws, government regulations, or changes to existing laws and regulations could make it difficult or impossible for us to obtain acceptable prices or adequate insurance coverage and reimbursement for Korlym, which would adversely affect our results of operations and financial position.
The commercial success of Korlym depends on the availability of acceptable pricing and adequate insurance coverage and reimbursement. Government payers, including Medicare, Medicaid and the Veterans Administration, as well as private insurers and health maintenance organizations, are increasingly attempting to contain healthcare costs by limiting reimbursement for medicines. In many foreign markets, drug prices and the profitability of prescription medications are subject to government control. In the United States, we expect that there will continue to be federal and state proposals for similar controls. Also, the trends toward managed health care in the United States and recent laws and legislation intended to increase the public visibility of drug prices and reduce the cost of government and private insurance programs could significantly influence the purchase of health care services and products and may result in lower prices for Korlym. If government or private payers cease to provide adequate and timely coverage, pricing and reimbursement for Korlym, physicians may not prescribe the medication and patients may not purchase it, even if it is prescribed, or the price we receive may be reduced, which would reduce our revenue.
In the United States, there have been and continue to be legislative initiatives to contain healthcare costs. The IRA significantly changed the way Medicare pays for prescription drugs. The IRA requires the Secretary of the U.S. Department of Health and Human Services (“HHS”) to negotiate Medicare prices for selected drugs and biologicals, including both physician-administered products covered under Medicare’s Part B benefit and self-administered drugs such as Korlym that are covered under the Part D benefit. Each year, the Secretary will select for price negotiation a specified number of negotiation-eligible drugs with the highest total Part B or D expenditures over the preceding 12-month period. To be eligible for price negotiation a drug must have been on the market for at least seven years without generic competition. Orphan drugs indicated for only one rare disease or condition and drugs with less than $200 million in annual Medicare expenditures are exempt from the negotiation program. For the first two years of the program, 2026 and 2027, only Part D drugs are eligible. The Secretary will publish the negotiated price, known as the “Maximum Fair Price” (“MFP”), for each of the selected products. Manufacturers of selected drugs would be required to offer the drug for Medicare recipients at the MFP. Manufacturers who fail to negotiate with the Secretary or offer their drug to Medicare recipients at the MFP can face significant civil money penalties or excise tax
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liability on sales of that drug. If Korlym or any drug we commercialize becomes eligible for Medicare negotiation, the revenue we generate from sales of that drug may be significantly reduced.
The IRA also establishes an inflation rebate program that requires manufacturers to pay rebates to the Medicare program if any of the medications they provide Medicare recipients increase in price faster than the rate of inflation. The Part D inflation rebate provision went into effect on October 1, 2022. Although manufacturers are generally familiar with inflation rebates under the Medicaid program, where they have existed for decades, the IRA represents the first time that inflation rebates have been extended to the Medicare program. The inflation rebate provision applies to any medication sold to Medicare recipients, whether or not that medication is subject to Medicare price negotiation.
Beginning in 2025, the IRA will also shift a significant portion of the Medicare beneficiary costs from the government and beneficiaries to manufacturers. We anticipate that this provision will significantly limit the revenue we receive and may materially reduce our revenue and profits.
We make grants to independent charitable foundations that help financially needy patients with their premium, co-pay, and co-insurance obligations with respect to their Cushing’s syndrome treatment, whether that treatment includes Korlym or not. There has been enhanced scrutiny of company-sponsored patient assistance programs, including insurance premium and co-pay assistance programs and donations to third-party charities that provide such assistance. As a result of this scrutiny, these assistance programs and charities may decide to reduce or eliminate entirely the assistance they provide to patients, which could result in fewer patients receiving the financial support they need to cover the cost of their Cushing’s syndrome care, including the cost of medication, which may include Korlym.
We expect governmental oversight and scrutiny of pharmaceutical companies to increase and that there will be additional attempts to change the healthcare system in ways that could harm our ability to sell Korlym and any other drugs we commercialize profitably, including new policies intended to curb healthcare costs, such as federal and state controls on reimbursement for drugs (including under Medicare and commercial health plans), new or increased requirements to pay prescription drug rebates and penalties to government health care programs and policies that require drug companies to disclose and justify the prices they charge.
Other companies offer different medications to treat patients with Cushing’s syndrome. The availability of competing treatments could limit our revenue from Korlym.
Since 2012, a medication owned by the Italian pharmaceutical company Recordati-S.p.A., the somatostatin analogue Signifor® (pasireotide) Injection, has been marketed in both the United States and the EU for adult patients with Cushing’s disease (a subset of Cushing’s syndrome). On March 6, 2020, the FDA granted Recordati approval to market another cortisol synthesis inhibitor, Isturisa® (osilodrostat) tablets, to treat patients with Cushing’s disease. Osilodrostat is approved in the EU for the treatment of patients with Cushing’s syndrome.
On December 30, 2021, Xeris received FDA approval to market the cortisol synthesis inhibitor Recorlev® (levoketoconazole) to treat patients with Cushing’s syndrome in the United States. Levoketoconazole is an enantiomer of the generic anti-fungal medication, ketoconazole, that is prescribed off-label to treat patients with Cushing’s syndrome.
Osilodrostat and levoketoconazole have been designated orphan drugs in both the EU and the United States.
Physician preference for any of these medications, or for the off-label use of generic medications such as ketoconazole, to treat patients with Cushing’s syndrome could reduce our revenue materially and harm our results of operations, which would cause our stock price to decline.
We depend on vendors to manufacture Korlym’s active ingredient, form it into tablets, package it and dispense it to patients. We also depend on vendors to manufacture the active pharmaceutical ingredient (“API”) and capsules or tablets for our product candidates. If our suppliers become unable or unwilling to perform these functions and we cannot transfer these activities to other vendors in a timely manner, our business will be harmed.
In the event any of our vendors fails to perform its contractual obligations to us or is materially impaired in its performance, we may experience disruptions and delays in our ability to deliver Korlym to patients or investigational drugs to patients in our clinical trials, which would adversely affect our business, results of operations and financial position.
Our single specialty pharmacy, Optime, dispenses Korlym and performs related pharmacy and patient support services, including the collection of payments from insurers representing more than 99 percent of our revenue. If Optime does not adhere to its agreements with payers or does not continue to meet regulatory requirements concerning pharmacy operations, it may not be able to collect on our behalf some or all of the payments due to us. In addition, if Optime becomes unable or unwilling to perform its obligations under our agreement, we may not be able to dispense Korlym in a timely manner to some or all of our
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patients. Effective April 1, 2024, we extended our agreement with Optime through March 31, 2027, with automatic renewal for successive three-year terms. The agreement is subject to customary termination provisions, including the right of Optime to terminate in the event of a material breach by us that we do not cure in a reasonable period of time after receiving written notice. In addition, we may terminate the agreement for convenience.
The facilities used by our vendors to manufacture and package the API and drug product for Korlym and our product candidates and distribute them to hospitals, clinics and patients, must be approved by government regulators in the United States, Europe, and elsewhere. We do not control the activities of these vendors, including whether they maintain adequate quality control and hire qualified personnel. We are dependent on them for compliance with the regulatory requirements known as current good manufacturing practices (“cGMPs”), which are subject to change at the regulators’ discretion. If our vendors cannot manufacture material that conforms to our specifications and the strict requirements of the FDA or others, they will not be able to maintain regulatory authorizations for their facilities and we could be prohibited from using the API or drug product they have provided. If the FDA, European Medicines Agency (“EMA”), the Medicines and Healthcare products Regulatory Agency (“MHRA”) or other regulatory authorities withdraw regulatory authorizations of these facilities, we may need to find alternative vendors or facilities, which would be time-consuming, complex and expensive and could significantly hamper our ability to develop, obtain regulatory approval for and market our products. Sanctions could be imposed on us, including fines, injunctions, civil penalties, refusal of regulators to approve our product candidates, delays, suspensions or withdrawals of approvals, seizures or recalls of products, operating restrictions and criminal prosecutions, any of which could harm our business. In addition, our reputation as a reliable sponsor of clinical studies would be harmed, which would make it more difficult for us to develop our drug candidates.
Natural disasters, such as earthquakes, fires, extreme weather events or widespread outbreaks of a deadly disease such as COVID-19, could disrupt our commercial and clinical activities or damage or destroy clinical trial sites, our office spaces, the residences of our employees or the facilities or residences of our vendors, contractors or consultants, which could significantly harm our operations.
A resurgence of COVID-19 or the widespread occurrence of another deadly illness could adversely affect our business, operations and financial results. The COVID-19 pandemic made it difficult to grow our commercial business and slowed the pace of some of our clinical trials.
We are also vulnerable to natural disasters, including earthquakes, fires, hurricanes, floods, blizzards and the extended periods of extreme heat, cold and precipitation made more frequent and severe by global warming. For example, our headquarters are in the San Francisco Bay Area, which experiences earthquakes, wildfires and flooding. Our specialty pharmacy, tablet manufacturers and warehouses are in areas subject to hurricanes and tornadoes. All our activities, as well as the activities of our vendors, consultants, clinical investigators, patients, physicians and regulators, are subject to the risks posed by global warming.
The loss of life, property damage and disruptions to electrical power distribution, communications, travel and shipping caused by natural disasters could make it difficult or impossible to conduct our commercial activities or complete our drug discovery activities or clinical trials. Patients may be unwilling or unable to travel to clinical trial sites, for example, or clinical materials or data may be lost.
Our insurance, if available at all, would likely be insufficient to cover losses resulting from disasters or other business interruptions.
If we are unable to maintain regulatory approval of Korlym or if we fail to comply with other requirements, we will be unable to generate revenue and may be subject to penalties.
We are subject to oversight by the FDA and other regulatory authorities in the United States and elsewhere with respect to our research, testing, manufacturing, labeling, distribution, adverse event reporting, storage, advertising, promotion, recordkeeping and sales and marketing activities. These requirements include submissions of safety information, annual updates on manufacturing activities and continued compliance with FDA regulations, including cGMPs, good laboratory practices and good clinical practices (“GCPs”), all of which are subject to change without notice and at the regulators’ sole discretion. Foreign regulatory authorities have comparable requirements and enforcement mechanisms, which are also subject to change. The FDA and other regulators enforce these regulations through inspections of us and the laboratories, manufacturers and clinical sites we use. Discovery of previously unknown problems with a product or product candidate, such as adverse events of unanticipated severity or frequency or deficiencies in manufacturing processes or management, as well as failure to comply with current or future FDA or other U.S. or foreign regulatory requirements, may subject us to substantial civil and criminal penalties, injunctions, holds on clinical trials, product seizure, refusal to permit the import or export of products, restrictions on product marketing, withdrawal of the product from the market, product recalls, total or partial suspension of production, refusal
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to approve pending new drug applications (“NDAs”) or supplemental NDAs, and suspension or revocation of product approvals.
We may be subject to civil or criminal penalties if our marketing of Korlym violates FDA regulations or health care fraud and abuse laws.
We are subject to FDA regulations governing the promotion and sale of medications. Although physicians are permitted to prescribe drugs for any indication they choose, manufacturers may only promote products for their FDA-approved use. All other uses are referred to as “off-label,” manufacturers are prohibited from engaging in any “off-label” promotion. In the United States, we market Korlym to treat hyperglycemia secondary to hypercortisolism in adult patients with endogenous Cushing’s syndrome who have type 2 diabetes mellitus or glucose intolerance and for whom surgery has failed or is not an option. Among other activities, we provide promotional materials and training programs to physicians covering the use of Korlym for this indication. The FDA may change its policies or enact new regulations at any time that may restrict our ability to promote our products, which could adversely impact our business.
If the FDA were to determine that we engaged in off-label promotion, the FDA could require us to change our practices and subject us to regulatory enforcement actions, including issuance of a public “warning letter,” untitled letter, injunction, seizure, civil fine or criminal penalties. Other federal or state enforcement authorities might act if they believe that the alleged improper promotion led to the submission and payment of claims for an unapproved use, which could result in significant fines or penalties under other statutory authorities, such as laws prohibiting false claims for reimbursement. Even if it is determined that we are not in violation of these laws, we may receive negative publicity, incur significant expenses and be forced to devote management time to defending our position.
In addition to laws prohibiting off-label promotion, we are also subject to federal and state healthcare fraud and abuse laws and regulations designed to prevent fraud, kickbacks, self-dealing and other abusive practices. The United States healthcare laws and regulations that may affect our ability to operate include, but are not limited to:
the federal Anti-Kickback Statute, which prohibits, among other things, knowingly and willfully soliciting, receiving, offering or paying remuneration, directly or indirectly, in exchange for or to induce either the referral of an individual for, or the purchase, order or recommendation of, any good or service for which payment may be made under federal health care programs such as Medicare and Medicaid. And, although we structure our applicable business arrangements in accordance with the safe harbors, it is difficult to determine exactly how the law will be applied in specific circumstances. Accordingly, it is possible that certain practices of ours may be challenged under the federal Anti-Kickback Statute. From a liability perspective, a person or entity does not need to have actual knowledge of the statute or specific intent to violate it in order to have committed a violation;
federal false claims laws, including, without limitation, the False Claims Act, which prohibit any person from knowingly presenting, or causing to be presented, a false claim for payment to the federal government, or knowingly making, or causing to be made, a false statement to get a false claim paid. The federal False Claims Act is unique in that it allows private individuals (whistleblowers) to bring actions on behalf of the federal government via qui tam actions. Importantly, under the False Claims Act the government may assert that a claim including items or services resulting from a violation of the federal Anti-Kickback Statute constitutes a false or fraudulent claim for purposes of the False Claims Act;
the federal Civil Monetary Penalties law, which prohibits, among other things, offering or transferring remuneration to a federal healthcare beneficiary that a person knows or should know is likely to influence the beneficiary’s decision to order or receive items or services reimbursable by the government from a particular provider or supplier;
HIPAA, which created federal criminal laws that prohibit executing a scheme to defraud any health care benefit program or making false statements relating to health care matters; similar to the federal Anti-Kickback Statute, a person or entity does not need to have actual knowledge of the statute or specific intent to violate it in order to have committed a violation;
federal “sunshine” laws, including the federal Physician Payment Sunshine Act (or sometimes referred to as the Open PaymentsTM Program), that require transparency regarding financial arrangements with health care providers, such as the reporting and disclosure requirements imposed by the Patient Protection and Affordable Care Act (“ACA”) on drug manufacturers regarding any “transfer of value” made or distributed to physicians, certain non-physician practitioners, teaching hospitals, and ownership or investment interests held by physicians and their immediate family members;
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federal consumer protection and unfair competition laws, which broadly regulate marketplace activities and activities that potentially harm consumers;
state law equivalents of each of the above federal laws, such as anti-kickback and false claims laws which may apply to items or services reimbursed by any third-party payer, including commercial insurers; state laws that require pharmaceutical companies to comply with the pharmaceutical industry’s voluntary compliance guidelines and the relevant compliance guidance promulgated by the federal government or otherwise restrict payments that may be made to healthcare providers; and
state laws that require drug manufacturers to report information related to payments and other transfers of value to physicians and other healthcare providers or marketing expenditures and pricing information.
The risk of being found in violation of these laws and regulations is increased by the fact that many of them have not been definitively interpreted by regulatory authorities or the courts and their provisions are open to a variety of interpretations. Because of the breadth of these laws and the narrowness of the statutory exceptions and safe harbors available under them, it is possible that some of our business activities, including our relationships with physicians and other healthcare providers (some of whom recommend, purchase and/or prescribe our products) and the manner in which we promote our products, could be subject to challenge and scrutiny. We are also exposed to the risk that our employees, independent contractors, principal investigators, consultants, vendors, distributors and contract research organizations (“CROs”) may engage in fraudulent or other illegal activity. Although we have policies and procedures prohibiting such activity, it is not always possible to identify and deter misconduct and the precautions we take may not be effective in controlling unknown risks or in protecting us from governmental investigations or other actions or lawsuits stemming from a failure to comply with applicable laws and regulations.
In November 2021, we received a records subpoena from the United States Attorney’s Office for the District of New Jersey (the “NJ USAO”) seeking information relating to the sale and promotion of Korlym, our relationships with and payments to health care professionals who can prescribe or recommend Korlym and prior authorizations and reimbursement for Korlym. The NJ USAO has informed us that it is investigating whether any criminal or civil violations by us occurred in connection with the matters referenced in the subpoena. It has also informed us that it does not currently consider us a defendant but rather an entity whose conduct is within the scope of the government’s investigation. We are cooperating with the investigation. Please see “Part II, Item 1, Legal Proceedings” for additional details.
If we are found in violation of any of the laws described above or any other government regulations, we may be subject to civil and criminal penalties, damages, fines, exclusion from governmental health care programs, a corporate integrity agreement or other agreement to resolve allegations of non-compliance, individual imprisonment, and the curtailment or restructuring of our operations, any of which could adversely affect our financial results and ability to operate.
Risks Related to our Research and Development Activities
Vendors perform many of the activities necessary to carry out our clinical trials, including drug product distribution, trial management and oversight and data collection and analysis. Failure of these vendors to perform their duties or meet expected timelines may prevent or delay approval of our product candidates.
Third-party clinical investigators and clinical sites enroll patients and CROs manage many of our trials and perform data collection and analysis. Although we control only certain aspects of these third parties’ activities, we are responsible for ensuring that every study adheres to its protocol and meets regulatory and scientific standards. If any of our vendors does not perform its duties or meet expected deadlines or fails to adhere to applicable GCPs, or if the quality or accuracy of the data it produces is compromised, affected clinical trials may be extended, delayed or terminated and we may be unable to obtain approval for our product candidates. Outside parties may have staffing difficulties, may undergo changes in priorities or may become financially distressed, adversely affecting their willingness or ability to conduct our clinical trials. Problems with the timeliness or quality of the work of a CRO may lead us to seek to terminate the relationship and use an alternative service provider. However, making this change may be costly and may delay our trials, and it may be challenging to find a replacement organization that can conduct our trials in an acceptable manner and at an acceptable cost. Failure of our manufacturing vendors to perform their duties or comply with cGMPs may require us to recall drug product or repeat clinical trials, which would delay regulatory approval. If our agreements with any of these vendors terminate, we may not be able to enter into alternative arrangements in a timely manner or on reasonable terms.
Our efforts to discover, develop and secure regulatory approval for our product candidates may not succeed. Clinical drug development is lengthy, expensive and often unsuccessful. Results of early studies and trials are often not predictive of later trial results. Failure can occur at any time. Even if we deem that our product candidates clinical trial
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results demonstrate safety and efficacy, regulatory authorities may not agree. Failure to obtain or maintain regulatory approvals for our product candidates would prevent us from commercializing them.
Clinical development is costly, time-consuming and unpredictable. Positive data from clinical trials are susceptible to varying interpretations, which could delay, limit or prevent regulatory approval. The results from early clinical trials are often not predictive of results in later clinical trials. Product candidates may fail to show the desired safety and efficacy traits despite having produced positive results in preclinical studies and initial clinical trials. Many companies have suffered significant setbacks in late-stage clinical trials due to lack of efficacy or unanticipated or unexpectedly severe adverse events.
Our current clinical trials may prove inadequate to support marketing approvals. Even trials that generate positive results may have to be confirmed in much larger, more expensive and lengthier trials before we could seek regulatory approval.
Clinical trials may take longer to complete, cost more than expected and fail for many reasons, including:
failure to show efficacy or acceptable safety;
slow patient enrollment or delayed activation of clinical trial sites;
delays obtaining regulatory permission to start a trial, changes to the size or design of a trial or changes in regulatory requirements for a trial already underway;
inability to secure acceptable terms with vendors and an appropriate number of clinical trial sites;
delays or inability to obtain institutional review board (“IRB”) approval at prospective trial sites;
failure of patients or investigators to comply with the clinical trial protocol;
unforeseen safety issues; and
negative findings of inspections of clinical sites or manufacturing operations by us, the FDA or other authorities.
A trial may also be suspended or terminated by us, the trial’s data safety monitoring board, the IRBs governing the sites where the trial is being conducted or the FDA for many reasons, including failure to comply with regulatory requirements or clinical protocols, negative findings in an inspection of our clinical trial operations or trial sites by the FDA or other authorities, unforeseen safety issues, failure to demonstrate a benefit or changes in government regulations.
At any time prior to the regulatory approval of a product candidate, we may decide, or the FDA or other regulatory authorities may require us, to conduct more pre-clinical or clinical studies, provide additional analysis of existing data or change the size or design of a trial already underway. Such additional or changed requirements, which regulators may impose in their sole discretion, may delay or prevent the completion of development, submission of an NDA or the completion of regulatory review, which would increase our costs and adversely impact future revenue. Even if we conduct the clinical trials and supportive studies that we consider appropriate and the results are positive, we may not receive regulatory approval. Following regulatory approval, there is no assurance of commercial success.
We may be unable to obtain or maintain regulatory approvals for our product or product candidates, which would prevent us from commercializing our product candidates.
We cannot sell a product without the approval of the FDA or comparable foreign regulatory authority. Obtaining such approval is difficult, uncertain, lengthy and expensive. Failure can occur at any stage. In order to receive FDA approval for a new drug, we must demonstrate to the FDA’s satisfaction that the new drug is safe and effective for its intended use and that our manufacturing processes comply with cGMPs. Our inability or the inability of our vendors to comply with applicable FDA and other regulatory requirements can result in delays in or denials of new product approvals, warning letters, untitled letters, fines, consent decrees restricting or suspending manufacturing operations, injunctions, civil penalties, recall or seizure of products, total or partial suspension of product sales and criminal prosecution. We may seek to commercialize our products in international markets, which would require us to receive a marketing authorization and, in many cases, pricing approval, from the appropriate regulatory authorities. Approval procedures vary between countries and can require additional pre-clinical or clinical studies. Obtaining approval may take longer than it does in the United States. Although approval by the FDA does not ensure approval by regulatory authorities in other countries, and approval by one foreign regulatory authority does not ensure approval by others, failure or delay in obtaining regulatory approval in one country may have a negative effect on the regulatory process in others. Any of these or other regulatory actions could materially harm our business and financial condition.
If we receive regulatory approval for a product candidate, we will be subject to ongoing requirements and oversight by the FDA and other regulatory authorities, such as continued safety and other reporting requirements and possibly post-approval
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marketing restrictions and additional costly clinical trials. If we are not able to maintain regulatory compliance, we may be required to stop development of a product candidate or to stop selling a product that has already been approved. We may also be subject to product recalls or seizures. Future governmental action or changes in regulatory authority policy or personnel may also result in delays or rejection of pending or anticipated product approvals.
Our products and product candidates may cause undesirable side effects that halt their clinical development, prevent their regulatory approval, limit their commercial potential or cause us significant liability.
Patients in clinical trials report changes in their health, including new illnesses, injuries and discomforts, to their study doctor. Often, it is not possible to determine whether or not these conditions were caused by the drug candidate being studied or something else. As we test our product candidates in larger, longer and more extensive clinical trials, or as use of them becomes more widespread if we receive regulatory approval, patients may report serious adverse events that did not occur or went undetected in previous trials. Many times, serious side effects are only detected in large-scale, Phase 3 clinical trials or following commercial approval.
Adverse events reported in clinical trials can slow or stop patient recruitment, prevent enrolled patients from completing a trial and could give rise to liability claims. Regulatory authorities could respond to reported adverse events by interrupting or halting our clinical trials or limiting the scope of, delaying or denying marketing approval. If we elect, or are required by authorities, to delay, suspend or terminate a clinical trial or commercialization efforts, the commercial prospects of the affected product candidates or products may be harmed and our ability to generate product revenues from them may be delayed or eliminated.
If one of our product candidates receives marketing approval, and we or others later identify undesirable side effects or adverse events, potentially significant negative consequences could result, including but not limited to:
regulatory authorities may suspend, limit or withdraw approvals of such product;
regulatory authorities may require additional warnings on the label, including “boxed” warnings, or issue safety alerts and other safety information about the product;
we may be required to change the way the product is administered or conduct additional studies or clinical trials;
we may be required to create a Risk Evaluation and Mitigation Strategy, which could include a medication guide outlining the risks of such side effects for distribution to patients, a communication plan for healthcare providers and/or other elements to assure safe use;
the product may become less competitive;
we may be subject to fines, injunctions or the imposition of criminal penalties; and
we could be sued and held liable for harm caused to patients.
Any of these events could seriously harm our business.
Risks Related to our Capital Needs and Financial Results
We may need additional capital to fund our operations or for strategic reasons. Such capital may not be available on acceptable terms or at all.
We are dependent on revenue from the sale of Korlym and our cash reserves to fund our commercial operations and development programs. If Korlym revenue declines significantly, we may need to curtail our operations or raise funds to support our plans. We may also choose to raise funds for strategic reasons. We cannot be certain funding will be available on acceptable terms or at all. Equity financing would cause dilution, debt financing may involve restrictive covenants. Neither type of financing may be available to us on attractive terms or at all. If we obtain funds through collaborations with other companies, we may have to relinquish rights to one or more of our product candidates. If our revenue declines and our cash reserves are depleted, and if adequate funds are not available from other sources, we may have to delay, reduce the scope of, or eliminate one or more of our development programs.
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Risks Relating to our Intellectual Property
To succeed, we must secure, maintain and effectively assert adequate patent protection for the composition and methods of use of our proprietary, selective cortisol modulators and for the use of Korlym to treat Cushing’s syndrome.
Patents are uncertain, involve complex legal and factual questions and are frequently the subject of litigation. The patents issued or licensed to us may be challenged at any time. Competitors may take actions we believe infringe our intellectual property, causing us to take legal action to defend our rights. Intellectual property litigation is lengthy, expensive and requires significant management attention. Outcomes are uncertain. If we do not protect our intellectual property, competitors may erode our competitive advantage. Please see “Part II, Item 1, Legal Proceedings” for additional information.
Our patent applications may not result in issued patents and patents issued to us may be challenged, invalidated, held unenforceable or circumvented. Our patents may not prevent third parties from producing competing products. The foreign countries where we may someday operate may not protect our intellectual property to the extent the laws of the United States do. If we fail to obtain adequate patent protection in other countries, others may produce products in those countries based on our technology.
Risks Related to our Stock
The price of our common stock fluctuates widely and is likely to continue to do so. Opportunities for investors to sell shares may be limited.
We cannot assure investors that a liquid trading market for our common stock will exist at any particular time. As a result, holders of our common stock may not be able to sell shares quickly or at the current market price. During the 52-week period ended October 23, 2024, our average daily trading volume was 1,105,185 shares and the intra-day sales prices per share of our common stock on The Nasdaq Stock Market ranged from $20.84 to $50.07. As of October 23, 2024, our officers, directors and principal stockholders beneficially owned 21 percent of our common stock.
Our stock price can experience extreme price and volume fluctuations that are unrelated or disproportionate to our operating performance or prospects. Securities class action lawsuits are often instituted against companies following periods of stock market volatility. Such litigation is costly and diverts management’s attention from productive efforts.
Factors that may cause the price of our common stock to fluctuate rapidly and widely include:
actual or anticipated variations in our operating results or changes to any public guidance we have provided;
actual or anticipated timing and results of our clinical trials;
actual or anticipated regulatory approvals of our product candidates;
disputes or other developments relating to our intellectual property, including developments in generic-related litigation;
changes in laws or regulations applicable to the pricing, availability of insurance reimbursement, or approved uses of Korlym, our product candidates or our competitors’ products;
short-selling of our common stock, the publication of negative opinions about our business or other market manipulation activities that are intended to lower our stock price or increase its volatility;
sales of a substantial number of shares of our stock in the public market, leading to reductions in its price;
changes in estimates or recommendations by securities analysts or the failure of our performance to meet the published expectations of those analysts or public guidance we have provided;
purchases of our common stock pursuant to our stock repurchase program (the “Stock Repurchase Program”) or changes to that program;
general market and economic conditions;
changes in the expected or actual timing of our competitors’ development programs and the approval of competing products;
purchases or sales of our common stock by our officers, directors or stockholders;
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technological innovations by us, our collaborators or our competitors;
conditions in the pharmaceutical industry, including the market valuations of companies similar to ours;
additions or departures of key personnel;
announcements by us or our competitors of significant acquisitions, strategic partnerships, joint ventures, collaborations or capital commitments; and
additional financing activities.
Our stock price may decline if our financial performance does not meet the guidance we have provided to the public, estimates published by research analysts or other investor expectations.
The guidance we provide as to our expected revenue is only an estimate of what we believe is realizable at the time we give such guidance. Our revenue depends on many factors, including, without limitation, the efficacy of our sales and marketing efforts, the price we receive from private and government payors, competition from alternate treatments for patients with Cushing’s syndrome, including from generic versions of Korlym and changes in government regulations. Our guidance estimate considers all of these factors, but they are difficult to predict. As a result, our revenue may vary materially from our guidance. Research analysts publish estimates of our future revenue and earnings based on their own analysis. The revenue guidance we provide may be one factor they consider when determining their estimates. If our revenue is materially less than the guidance we or the research analysts who cover our stock provide investors, our stock price may decline.
We have in the past and may in the future be subject to short selling strategies that may drive down the market price of our common stock and increase its volatility.
Short sellers have, and likely will continue to, attempt to drive down the price of our common stock. Short selling is the practice of selling stock the seller does not own with the intention of buying it back later at a lower price, thereby profiting from any decline in the price of the stock between the time it is sold and the time it is repurchased. To support their efforts, short sellers often publish, or arrange for others to publish, negative opinions regarding the relevant issuer and its business prospects. These publications are often made to appear as if they were objective journalism or unbiased “research reports” of the type distributed by credible Wall Street firms and independent research analysts. Short seller publications are not regulated by any governmental, self-regulatory organization or other authority in the United States and the opinions they express are often based on distortions, omissions or fabrications. Short attacks supported by such publications have, in the past, led to selling of our stock and at least temporary reductions in its price. Companies that are subject to unfavorable allegations, even if untrue, may have to expend a significant amount of resources to investigate such allegations and/or defend themselves, including shareholder suits against the company that may be prompted by such allegations. We have been, and may in the future be, the subject of shareholder suits prompted by allegations made by short sellers.
General Risk Factors
We need to increase the size of our organization and may experience difficulties in managing growth.
Our commercial and research and development efforts are constrained by our limited administrative, operational and management resources. To date, we have relied on a small management team. Growth will impose significant added responsibilities on members of management, including the need to recruit and retain additional employees. Our financial performance and ability to compete will depend on our ability to manage growth effectively. To that end, we must:
continue to add talented, experienced personnel to our endocrine, oncology and emerging markets businesses;
manage our clinical trials, research and manufacturing activities effectively;
hire more general management, clinical development, administrative and sales and marketing personnel; and
continue to develop our administrative systems and controls.
Failure to accomplish any of these tasks could harm our business.
If we lose key personnel or are unable to attract more skilled personnel, we may be unable to pursue our product development and commercialization goals.
Our ability to operate successfully and manage growth depends upon hiring and retaining skilled managerial, scientific, sales, marketing and financial personnel. The job market for qualified personnel is intensely competitive and turnover rates
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have reached record highs within our industry and the geographical areas from which we recruit. We depend on the principal members of our management and scientific staff. Any officer or employee may terminate his or her relationship with us at any time and work for a competitor. We do not have employment insurance covering any of our personnel. The loss of key individuals could delay our research, development and commercialization efforts.
We are subject to regulations and other legal obligations relating to drug development and commercialization, the conduct of business as an issuer of publicly traded securities and individual privacy and data protection. Compliance with these obligations is complex and costly. Failure to comply could materially harm our business.
New laws and regulations, as well as changes to existing laws and regulations, including statutes and regulations concerning taxes and the development, approval, marketing and pricing of medications, the provisions of the ACA requiring the reporting of aggregate spending related to health care professionals, the provisions of the Sarbanes-Oxley Act of 2002, the Dodd Frank Act of 2010 and rules adopted by the SEC and by The Nasdaq Stock Market have and will likely continue to increase our cost of doing business and divert management’s attention from revenue-generating activities.
We and our partners are subject to federal, state and foreign laws and regulations concerning data privacy and security, including HIPAA and the EU General Data Protection Regulation (“GDPR”). These and other regulatory frameworks are evolving rapidly as new rules are enacted and existing ones updated and made more stringent.
In the United States, numerous federal and state laws and regulations, including state data breach notification laws, state health information privacy, laws, and federal and state consumer protection laws and regulations (e.g., Section 5 of the Federal Trade Commission Act), that govern the collection, use, disclosure, and protection of health-related and other personal information could apply to our operations or the operations of our partners. In addition, we may obtain health information from third parties (including research institutions from which we obtain clinical trial data) that are subject to privacy and security requirements under HIPAA. Depending on the facts and circumstances, we could be subject to criminal penalties if we knowingly obtain, use, or disclose individually identifiable health information maintained by a HIPAA-covered entity in a manner that is not authorized or permitted by HIPAA.
Even when HIPAA does not apply, according to the Federal Trade Commission (the “FTC”), violating consumers’ privacy or failing to take appropriate steps to keep consumers’ personal information secure may constitute unfair acts or practices in or affecting commerce in violation of Section 5(a) of the Federal Trade Commission Act. The FTC expects a company’s data security measures to be reasonable and appropriate in light of the sensitivity and volume of consumer information it holds, the size and complexity of its business, and the cost of available tools to improve security and reduce vulnerabilities. Individually identifiable health information is considered sensitive data that merits stronger safeguards. In 2022, the FTC also began a rulemaking proceeding to develop additional data privacy rules and requirements, which may add additional complexity to compliance obligations going forward.
In addition, certain state laws govern the privacy and security of health information in certain circumstances, some of which are more stringent than HIPAA and many of which differ from each other in significant ways and may not have the same effect, thus complicating compliance efforts. Failure to comply with these laws, where applicable, can result in the imposition of significant civil and/or criminal penalties and private litigation. For example, the California Confidentiality of Medical Information Act imposes restrictive requirements regulating the use and disclosure of health information and other personally identifiable information. Further, the California Consumer Privacy Act, or the CCPA, which took effect on January 1, 2020, created individual privacy rights for California consumers and increased the privacy and security obligations of entities handling certain personal information. The CCPA provides for civil penalties for violations, as well as a private right of action for data breaches that is expected to increase data breach litigation. The CCPA may increase our compliance costs and potential liability. Further, the California Privacy Rights Act, or CPRA, revised and expanded the CCPA, adding additional data protection obligations on covered businesses, including additional consumer rights processes, limitations on data uses, new audit requirements for higher risk data, and opt outs for certain uses of sensitive data. It also created a new California data protection agency authorized to issue substantive regulations and could result in increased privacy and information security enforcement. The CPRA is in full effect as of January 1, 2023, and similar laws passed in Virginia, Colorado, Connecticut and Utah have taken effect and other states, including Texas, Florida, Oregon and Montana, have passed similar laws that will take effect in or after 2024. As a result, additional compliance investment and potential business process changes may be required. In the event that we are subject to or affected by HIPAA, the CCPA, the CPRA or other domestic privacy and data protection laws, any liability from failure to comply with the requirements of these laws could adversely affect our financial condition. Additional legislation proposed at the federal level and in other states, along with increased regulatory action, reflect a trend toward more stringent privacy legislation in the United States.
Outside the United States, many jurisdictions have or are in the process of enacting sweeping data privacy regulatory regimes. In Europe, the GDPR took effect in 2018, and is imposing stringent requirements for controllers and processors of
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personal data of individuals within the EEA, particularly with respect to clinical trials. The GDPR provides that EEA member states may make their own further laws and regulations limiting the processing of health data, which could limit our ability to use and share personal data or could cause our costs to increase and harm our business and financial condition. In addition, the GDPR increases the scrutiny that clinical trial sites located in the EEA should apply to transfers of personal data from such sites to countries that are considered to lack an adequate level of data protection, such as the United States. Recent legal developments have added complexity and compliance uncertainty regarding certain transfers of information from the EEA to the United States. Following EU court decisions, updated standard contractual clauses (“SCCs”) were adopted to account for these judicial decisions, imposing new requirements on data transfers. The revised SCCs must be used for relevant new data transfers from September 27, 2021, and existing SCC arrangements were required to be migrated by December 27, 2022. There is some uncertainty around whether the revised clauses can be used for all types of data transfers, particularly whether they can be relied on for data transfers to non-EEA entities subject to the GDPR. As supervisory authorities issue further guidance on personal data export mechanisms, including circumstances where the SCCs cannot be used, and/or start taking enforcement action, we could suffer additional costs, complaints and/or regulatory investigations or fines, and/or if we are otherwise unable to transfer personal data between and among countries and regions in which we operate, it could affect the manner in which we provide our services, the geographical location or segregation of our relevant systems and operations, and could adversely affect our financial results. The GDPR imposes substantial fines for breaches of data protection requirements, which can be up to four percent of global revenue for the preceding financial year or €20 million, whichever is greater, and it also confers a private right of action on data subjects for breaches of data protection requirements. Compliance with European data protection laws is a rigorous and time intensive process that may increase our cost of doing business, and despite those efforts, there is a risk that we may be subject to fines and penalties, litigation and reputational harm in connection with our European activities. From January 1, 2021, we have had to comply with the GDPR and separately the United Kingdom GDPR, which, together with the amended United Kingdom Data Protection Act 2018, retains the GDPR in United Kingdom national law, each regime having the ability to fine up to the greater of €20 million/ £17.5 million or 4 percent of global turnover. It is unclear how United Kingdom data protection laws and regulations will develop in the medium to longer term and these changes may lead to additional costs and increase our overall risk exposure. On June 28, 2021, the EC adopted an adequacy decision in favor of the United Kingdom, enabling data transfers from EU member states to the United Kingdom without additional safeguards. However, the United Kingdom adequacy decision will automatically expire in June 2025 unless the EC renews or extends that decision and remains under review by the Commission during this period.
Complying with U.S. and foreign privacy and security laws and regulations is complex and costly. Failure to comply by us or our vendors could subject us to litigation, government enforcement actions and substantial penalties and fines, which could harm our business.
We rely on information technology to conduct our business. A breakdown or breach of our information technology systems or our failure to protect confidential information concerning our business, patients or employees could interrupt the operation of our business and subject us to liability.
We store valuable confidential information relating to our business, patients and employees on our computer networks and on the networks of our vendors. In addition, we rely heavily on internet technology, including video conference, teleconference and file-sharing services, to conduct business. Despite our security measures, our networks and the networks of our vendors are at risk of break-ins, installation of malware or ransomware, denial-of-service attacks, data theft and other forms of malfeasance by persons seeking to commit fraud or theft, which could result in unauthorized access to, and/or misuse of, our clinical data or other confidential information, including confidential information relating to our patients or employees. We may continue to increase our cybersecurity risks, due to our reliance on internet technology and the number of our employees that are working remotely, which may create additional opportunities for cybercriminals to exploit vulnerabilities.
We and our vendors have experienced data breaches, theft, “phishing” attacks and other unauthorized access to confidential data and information. There can be no assurance that our cybersecurity systems and processes will prevent unauthorized access in the future that causes serious harm to us, our patients or employees. We may also experience security breaches that remain undetected for an extended period.
Disruptions or security breaches that result in the disclosure of confidential or proprietary information could cause us to incur liability and delay or otherwise harm our research, development and commercialization efforts. We may be liable for losses suffered by patients or employees or other individuals whose confidential information is stolen as a result of a breach of the security of the systems that we or third parties and our vendors store this information on, and any such liability could be material. Even if we are not liable for such losses, any breach of these systems could expose us to material costs in notifying affected individuals, as well as regulatory fines or penalties. In addition, any breach of these systems could disrupt our normal business operations and expose us to reputational damage and harm our business, operating results and financial condition. Any insurance we maintain against the risk of this type of loss may not be sufficient to cover actual losses or may not apply to the circumstances relating to any particular loss.
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Changes in federal, state and local tax laws may reduce our net earnings.
Our earnings are subject to federal, state and local taxes. We offset a portion of our earnings using net operating losses and our taxes using research and development tax credits, which reduces the amount of tax we pay. Some jurisdictions require that we pay taxes or fees calculated as a percentage of sales, payroll expense, or other indicia of our activities. Please see “Part I, Item 1, Notes to Unaudited Condensed Consolidated Financial Statements – Income Taxes.” Changes to existing tax laws could materially increase the amounts we pay, which would reduce our after tax net income.
Research analysts may not continue to provide or initiate coverage of our common stock or may issue negative reports.
The market for our common stock may be affected by the reports financial analysts publish about us. If any of the analysts covering us downgrades or discontinues coverage of our stock, the price of our common stock could decline rapidly and significantly. Paucity of research coverage may also adversely affect our stock price.
Any acquisition of Corcept shares through our stock repurchase program or, in certain cases, pursuant to the exercise of stock options, will reduce our cash reserves.
In January 2024, our Board of Directors authorized the repurchase of up to $200 million of our common stock pursuant to the Stock Repurchase Program. In addition, we sometimes accept, in our sole discretion, shares equal in value to any tax and exercise price liability due from option holders at the time of exercise and remit the applicable tax amounts to the tax authorities. Neither our Stock Repurchase Program nor the acceptance of shares at the time of options exercise require us to acquire shares. Furthermore, the Stock Repurchase Program may be modified, suspended or discontinued at any time without notice. It is possible that other uses of our capital would have been more advantageous or that our future capital requirements increase unexpectedly. By reducing our cash balance, our repurchases of common stock could hamper our ability to execute our plans, meet financial obligations or access financing.
Anti-takeover provisions in our charter and bylaws and under Delaware law may make an acquisition of us or a change in our management more expensive or difficult, even if an acquisition or a management change would be beneficial to our stockholders.
Provisions in our charter and bylaws may delay or prevent an acquisition of us or a change in our management. Some of these provisions allow us to issue preferred stock without any vote or further action by the stockholders, require advance notification of stockholder proposals and nominations of candidates for election as directors and prohibit stockholders from acting by written consent. In addition, a supermajority vote of stockholders is required to amend our bylaws. Our bylaws provide that special meetings of the stockholders may be called only by our Chairman, President or the Board of Directors and that the authorized number of directors may be changed only by resolution of the Board of Directors. These provisions may prevent or delay a change in our Board of Directors or our management, which our Board of Directors appoints. In addition, because we are incorporated in Delaware, we are governed by the provisions of Section 203 of the Delaware General Corporation Law. Section 203 may prohibit large stockholders, in particular those owning 15 percent or more of our outstanding voting stock, from merging or combining with us. These provisions in our charter and bylaws and under Delaware law could reduce the price that investors would be willing to pay for shares of our common stock.
Our officers, directors and principal stockholders, acting as a group, could significantly influence corporate actions.
As of October 23, 2024, our officers and directors beneficially owned 21 percent of our common stock. Acting together, these stockholders could significantly influence any matter requiring approval by our stockholders, including the election of directors and the approval of mergers or other business combinations. The interests of this group may not always coincide with our interests or the interests of other stockholders and may prevent or delay a change in control. This significant concentration of share ownership may adversely affect the trading price of our common stock because many investors perceive disadvantages to owning stock in companies with controlling stockholders.
ITEM 2.  UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
There were no unregistered sales of equity securities during the period covered by this report.
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Issuer Purchases of Equity Securities
The following table contains information relating to the repurchases of our common stock in the three months ended September 30, 2024 as part of our publicly announced stock repurchase program (in thousands, except average price per share):
Fiscal PeriodTotal Number of Shares RepurchasedAverage Price Paid Per Share
Dollar Amount of Shares That May Yet be Purchased Under the Program(1)
July 1, 2024 to July 31, 2024— $— $— 
August 1, 2024 to August 31, 2024270 34.03 186,842 
September 1, 2024 to September 30, 202474 33.97 184,329 
Total344 $34.02 $184,329 
(1) On January 8, 2024, our Board of Directors authorized the repurchase of up to $200 million of our common stock pursuant to our Stock Repurchase Program. The program may be modified, suspended or discontinued at any time without notice.
The following table contains information relating to the purchases of our common stock in the three months ended September 30, 2024 as part of the cashless net exercises of stock options (in thousands, except average price per share):

Fiscal Period
Total Number of Shares Purchased(1)
Average Price Per Share
Total Purchase Price of Shares(2)
July 1, 2024 to July 31, 2024322 $37.82 $12,175 
August 1, 2024 to August 31, 2024116 36.23 4,218 
September 1, 2024 to September 30, 202488 37.82 3,311 
Total526 $37.47 $19,704 
(1) In July 2024, we issued 518,670 shares of common stock as part of a net-share settlement of a cashless option exercise, of which 315,870 shares were surrendered to us in satisfaction of related exercise cost and tax obligations. In August 2024, we issued 217,081 shares of common stock as part of a net-share settlement of a cashless option exercise, of which 99,831 shares were surrendered to us. In September 2024, we issued 156,227 shares of common stock as part of a net-share settlement of a cashless option exercise, of which 78,239 shares were surrendered to us.
In July 2024, we issued 17,023 shares of common stock as part of restricted stock vesting, of which 6,070 shares were surrendered to us in satisfaction of related tax obligations. In August 2024, we issued 46,575 shares of common stock as part of restricted stock vesting, of which 16,601 shares were surrendered to us. In September 2024, we issued 26,924 shares of common stock as part of restricted stock vesting, of which 9,323 shares were surrendered to us.
(2) We paid $11.7 million to satisfy the tax withholding obligations associated with the net-share settlement of these cashless option exercises and vesting of restricted stock.
ITEM 3.  DEFAULTS UPON SENIOR SECURITIES
Not applicable.
ITEM 4.  MINE SAFETY DISCLOSURES
Not applicable.
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ITEM 5.  OTHER INFORMATION
Insider Trading Arrangements
During the quarter ended September 30, 2024, none of our directors and officers (as defined in Rule 16a-1(f) under the Exchange Act) adopted or terminated any contract, instruction or written plan for the purchase or sale of our securities that are intended to satisfy the affirmative defense conditions of Rule 10b5-1(c) of the Securities Exchange Act of 1934, as amended, or any “non-Rule 10b5-1 trading arrangement,” as defined in Item 408(a) of Regulation S-K, other than as set forth in the table below.
NamePositionActionAdoption DateTotal Shares of Common Stock to be Sold
Expiration Date(1)
Daniel SwisherDirectorAdoption8/1/2024
Up to 26,400
10/13/2025
Joseph D. LyonChief Accounting and Technology OfficerAdoption8/30/2024
Up to 260,000
12/31/2025
Sean MaduckPresident, EndocrinologyAdoption9/5/2024
Up to 340,000
12/31/2025
(1) Each trading arrangement permits transactions through and including the earlier to occur of (a) the completion of all sales or (b) the date listed in the table.
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ITEM 6.  EXHIBITS
Exhibit
Number
 Description of Document
3.1 
3.2 
31.1 
31.2 
32.1 
32.2 
101 
The following materials from the registrant’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2024, formatted in Extensible Business Reporting Language (XBRL): (i) Unaudited Condensed Consolidated Balance Sheets at September 30, 2024 and December 31, 2023, (ii) Unaudited Condensed Consolidated Statements of Income for the three and nine month periods ended September 30, 2024 and 2023, (iii) Unaudited Condensed Consolidated Statements of Comprehensive Income for the three and nine month periods ended September 30, 2024 and 2023, (iv) Unaudited Condensed Consolidated Statements of Cash Flows for the nine month periods ended September 30, 2024 and 2023, (v) Unaudited Condensed Consolidated Statement of Stockholders’ Equity and (vi) Notes to Unaudited Condensed Consolidated Financial Statements.
104Cover Page Interactive Data File - the cover page XBRL tags are embedded within the Inline XBRL document.

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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
 CORCEPT THERAPEUTICS INCORPORATED
  
Date: October 30, 2024/s/ Joseph K. Belanoff
 Joseph K. Belanoff, M.D.
Chief Executive Officer
  
Date:
October 30, 2024/s/Atabak Mokari
 Atabak Mokari
 Chief Financial Officer
Date:October 30, 2024/s/Joseph D. Lyon
Joseph D. Lyon
Chief Accounting & Technology Officer

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