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Jasper Therapeutics Announces First Patient Dosed in Phase 1b/2a SPOTLIGHT Clinical Study of Briquilimab in Chronic Inducible Urticaria

Jasper Therapeutics Announces First Patient Dosed in Phase 1b/2a SPOTLIGHT Clinical Study of Briquilimab in Chronic Inducible Urticaria

Jasper Therapeutics宣布在治疗慢性诱发性荨麻疹的1b/2a期临床研究中为首位患者服用剂量
Jasper Therapeutics ·  03/19 12:00

REDWOOD CITY, Calif., March 19, 2024 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (Jasper), a biotechnology company focused on development of briquilimab, a novel antibody therapy targeting c-Kit (CD117) in mast cell driven diseases such as chronic spontaneous urticaria (CSU) and chronic inducible urticaria (CIndU), today announced that the first patient has been dosed in Jasper's Phase 1b/2a (SPOTLIGHT) clinical study of subcutaneous briquilimab for the treatment of CIndU. The SPOTLIGHT study is evaluating a single administration, at two different dose levels, of subcutaneous briquilimab in adult patients with cold urticaria (ColdU) or symptomatic dermographism (SD).

加利福尼亚州雷德伍德城,2024年3月19日(GLOBE NEWSWIRE)——专注于开发briquilimab的生物技术公司Jasper Therapeutics, Inc.(纳斯达克股票代码:Jsper)(Jasper)今天宣布,这是一种针对慢性自发性荨麻疹(CSU)和慢性诱发性荨麻疹(CindU)等肥大细胞驱动疾病的C-kit(CD117)的新型抗体疗法在贾斯珀的皮下布里曲利单抗治疗CindU的1b/2a期(SPOTLIGHT)临床研究中,第一位患者已经服用了剂量。SPOTLIGHT研究正在评估在感冒性荨麻疹(ColDU)或有症状的皮肤造影术(SD)的成年患者中,在两种不同的剂量水平下单次使用briquilimab。

"We are excited to announce dosing of the first patient in the SPOTLIGHT study in patients with CIndU, our second clinical program evaluating briquilimab in a mast cell-mediated disease," said Edwin Tucker, Chief Medical Officer of Jasper. "As with our BEACON study in CSU, we expect the SPOTLIGHT study to establish proof of concept for the depletion of mast cells by briquilimab in CIndU and help us to determine doses and dosing regimens for future registrational studies. We plan to provide enrollment updates as we progress through the study and anticipate reporting preliminary data in the second half of 2024."

贾斯珀首席医学官埃德温·塔克说:“我们很高兴地宣布,SPOTLIGHT研究中的第一位患者在CindU患者中给药,这是我们第二个评估briquilimab治疗肥大细胞介导疾病的临床项目。”“与我们在科罗拉多州立大学的BEACON研究一样,我们预计SPOTLIGHT研究将为briquilimab在CindU中消耗肥大细胞提供概念验证,并帮助我们为未来的注册研究确定剂量和给药方案。随着研究的进展,我们计划提供最新入学情况,并预计将在2024年下半年报告初步数据。”

The SPOTLIGHT study is expected to enroll approximately 15 patients across 2 dose cohorts. The primary endpoints are safety and tolerability of briquilimab with secondary endpoints focused on efficacy measures and pharmacokinetics. The study is being conducted at four sites in the EU. Jasper anticipates reporting preliminary data from the SPOTLIGHT study in the second half of 2024.

SPOTLIGHT研究预计将在2个剂量队列中招收约15名患者。主要终点是briquilimab的安全性和耐受性,次要终点侧重于疗效指标和药代动力学。该研究正在欧盟的四个地点进行。贾斯珀预计将在2024年下半年报告SPOTLIGHT研究的初步数据。

"c-Kit inhibitors are a promising class of monoclonal therapeutics with demonstrated efficacy in mast cell driven diseases," said Marcus Maurer, M.D., Professor of Dermatology and Allergy at Charité – Universitätsmedizin in Berlin. "As a potent and differentiated c-Kit inhibitor, I believe briquilimab has the potential to serve as an important treatment option for patients suffering from CIndU, and I look forward to enrolling patients into the SPOTLIGHT study and additionally into the BEACON study for CSU."

柏林查里特大学皮肤病学和过敏学教授马库斯·毛雷尔医学博士说:“C-kit抑制剂是一类前景看好的单克隆疗法,在肥大细胞驱动的疾病中已显示出疗效。”“作为一种有效的差异化C-kit抑制剂,我相信briquilimab有可能成为CindU患者的重要治疗选择,我期待着让患者参与SPOTLIGHT研究以及科罗拉多州立大学的BEACON研究。”

About Briquilimab

关于 briquilimab

Briquilimab (formerly JSP191) is a targeted aglycosylated monoclonal antibody that blocks stem cell factor from binding to the cell-surface receptor c-Kit, also known as CD117, thereby inhibiting signaling through the receptor. This inhibition disrupts the critical survival signal, leading to the depletion of the mast cells via apoptosis which removes the underlying source of the inflammatory response in mast cell driven diseases such as chronic urticaria. Jasper is currently conducting clinical studies of briquilimab as a treatment in patients with CSU or with CIndU. Briquilimab is also currently in clinical studies as a treatment for patients with LR-MDS and as a conditioning agent for cell therapies for rare diseases. To date, briquilimab has a demonstrated efficacy and safety profile in more than 145 dosed participants and healthy volunteers, with clinical outcomes as a conditioning agent in severe combined immunodeficiency (SCID), AML, MDS, FA, and sickle cell disease (SCD).

Briquilimab(前身为 JSP191)是一种靶向的糖基化单克隆抗体,可阻止干细胞因子与细胞表面受体 C-kit(也称为 CD117)结合,从而抑制通过受体的信号传导。这种抑制会干扰关键的存活信号,通过细胞凋亡导致肥大细胞消耗,从而消除肥大细胞驱动的疾病(例如慢性荨麻疹)炎症反应的潜在来源。贾斯珀目前正在对briquilimab作为科罗拉多州立大学或CinDU患者的治疗药物进行临床研究。Briquilimab目前也在临床研究中,它既是LR-MDS患者的治疗方法,也是罕见疾病细胞疗法的调理剂。迄今为止,briquilimab在超过145名给药参与者和健康志愿者中具有显著的疗效和安全性,作为重度联合免疫缺陷(SCID)、急性髓细胞白血病、MDS、FA和镰状细胞病(SCD)的调理剂具有临床疗效。

About Jasper

关于贾斯珀

Jasper is a clinical-stage biotechnology company developing briquilimab, a monoclonal antibody targeting c-Kit (CD117) as a therapeutic for chronic mast and stem cell diseases such as chronic urticaria and lower to intermediate risk MDS and as a conditioning agent for stem cell transplants for rare diseases such as SCD, FA and SCID. To date, briquilimab has a demonstrated efficacy and safety profile in more than 145 dosed participants and healthy volunteers, with clinical outcomes as a conditioning agent in SCID, AML, MDS, FA, and SCD. For more information, please visit us at www.jaspertherapeutics.com.

Jasper是一家处于临床阶段的生物技术公司,正在开发briquilimab,这是一种靶向 c-kit (CD117) 的单克隆抗体,用于治疗慢性荨麻疹和低至中等风险 MDS 等慢性肥大和干细胞疾病,并作为 SCD、FA 和 SCID 等罕见疾病干细胞移植的调节剂。迄今为止,briquilimab在超过145名给药参与者和健康志愿者中已得到证实的疗效和安全性,作为SCID、AML、MDS、FA和SCD的调理剂,其临床结果为调理剂。欲了解更多信息,请访问我们的网站 www.jaspertherapeut

Forward-Looking Statements

前瞻性陈述

Certain statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied by words such as "believe," "may," "will," "estimate," "continue," "anticipate," "intend," "expect," "should," "would," "plan," "predict," "potential," "seem," "seek," "future," "outlook" and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding briquilimab's potential, including with respect to its potential in mast cell driven diseases such as CSU and CIndU and its potential to serve as an important treatment option for patients suffering from CIndU; Jasper's expectations regarding its Phase 1b/2a SPOTLIGHT study of subcutaneous briquilimab in CIndU, including the expected enrollment, cohorts and site locations, the expected timing for reporting preliminary data, the expectation that the SPOTLIGHT or BEACON studies will establish proof of concept or help Jasper determine doses and dosing regimens for future registrational studies; and Jasper's expectations regarding its BEACON study in CSU, including the expectation that Jasper will enroll additional patients in the BEACON study for CSU. These statements are based on various assumptions, whether or not identified in this press release, and on the current expectations of Jasper and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied on by an investor as, a guarantee, an assurance, a prediction or a definitive statement of fact or probability. Many actual events and circumstances are beyond the control of Jasper. These forward-looking statements are subject to a number of risks and uncertainties, including general economic, political and business conditions; the risk that the potential product candidates that Jasper develops may not progress through clinical development or receive required regulatory approvals within expected timelines or at all; the risk that clinical trials may not confirm any safety, potency or other product characteristics described or assumed in this press release; the risk that Jasper will be unable to successfully market or gain market acceptance of its product candidates; the risk that prior study results may not be replicated; the risk that Jasper's product candidates may not be beneficial to patients or successfully commercialized; patients' willingness to try new therapies and the willingness of physicians to prescribe these therapies; the effects of competition on Jasper's business; the risk that third parties on which Jasper depends for laboratory, clinical development, manufacturing and other critical services will fail to perform satisfactorily; the risk that Jasper's business, operations, clinical development plans and timelines, and supply chain could be adversely affected by the effects of health epidemics; the risk that Jasper will be unable to obtain and maintain sufficient intellectual property protection for its investigational products or will infringe the intellectual property protection of others; and other risks and uncertainties indicated from time to time in Jasper's filings with the SEC, including its Annual Report on Form 10-K for the year ended December 31, 2023 and subsequent Quarterly Reports on Form 10-Q. If any of these risks materialize or Jasper's assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. While Jasper may elect to update these forward-looking statements at some point in the future, Jasper specifically disclaims any obligation to do so. These forward-looking statements should not be relied upon as representing Jasper's assessments of any date subsequent to the date of this press release. Accordingly, undue reliance should not be placed upon the forward-looking statements.

就1995年《美国私人证券诉讼改革法》的安全港条款而言,本新闻稿中包含的某些非历史事实的陈述是前瞻性陈述。前瞻性陈述有时伴随着诸如 “相信”、“可能”、“将”、“估计”、“继续”、“预测”、“打算”、“预期”、“应该”、“将”、“计划”、“潜在”、“看来”、“寻找”、“未来”、“展望” 等词语以及预测或表明未来事件或趋势或不是历史问题陈述的类似表达。这些前瞻性陈述包括但不限于有关briquilimab潜力的陈述,包括其在科罗拉多州立大学和CindU等肥大细胞驱动疾病中的潜力及其作为CindU患者重要治疗选择的潜力;贾斯珀对CindU皮下briquilimab的1b/2a期SPOTLIGHT研究,包括预期入组、队列和研究地点的预期,报告初步数据的预期时间,SPOTLIGHT或BEACON研究的期望将建立概念验证或帮助贾斯珀确定未来注册研究的剂量和给药方案;以及贾斯珀对科罗拉多州立大学BEACON研究的期望,包括预计贾斯珀将在科罗拉多州立大学的BEACON研究中招收更多患者。这些陈述基于各种假设,无论是否在本新闻稿中提出,也基于贾斯珀当前的预期,不是对实际业绩的预测。这些前瞻性陈述仅用于说明目的,无意用作担保、保证、预测或明确的事实或概率陈述,投资者也不得依赖这些陈述作为担保、保证、预测或明确的事实或概率陈述。许多实际事件和情况都超出了贾斯珀的控制范围。这些前瞻性陈述受许多风险和不确定性的影响,包括总体经济、政治和商业状况;贾斯珀开发的潜在候选产品可能无法在预期的时间表内或根本无法通过临床开发取得进展或获得所需的监管部门批准的风险;临床试验可能无法证实本新闻稿中描述或假设的任何安全性、效力或其他产品特征的风险;贾斯珀无法成功上市或获得市场认可的风险其候选产品;先前研究结果无法复制的风险;贾斯珀的候选产品可能无法使患者受益或无法成功商业化的风险;患者尝试新疗法的意愿和医生开这些疗法的意愿;竞争对贾斯珀业务的影响;贾斯珀赖以提供实验室、临床开发、制造和其他关键服务的第三方无法令人满意地表现的风险;贾斯珀的风险 Per 的业务、运营、临床发展计划和时间表以及供应链可能会受到以下因素的不利影响:健康流行病的影响;贾斯珀无法为其研究产品获得和维持足够的知识产权保护或侵犯他人知识产权保护的风险;以及贾斯珀向美国证券交易委员会提交的文件中不时指出的其他风险和不确定性,包括其截至2023年12月31日止年度的10-K表年度报告和随后的表格季度报告 10-Q。如果其中任何风险得以实现或贾斯珀的假设被证明不正确,则实际结果可能与这些前瞻性陈述所暗示的结果存在重大差异。尽管贾斯珀可能会选择在未来的某个时候更新这些前瞻性陈述,但贾斯珀明确表示不承担任何更新这些前瞻性陈述的义务。不应将这些前瞻性陈述视为贾斯珀对本新闻稿发布之日后任何日期的评估。因此,不应过分依赖前瞻性陈述。

Contacts:

联系人:

Joyce Allaire (investors)
LifeSci Advisors
617-435-6602
jallaire@lifesciadvisors.com

乔伊斯·阿莱尔(投资者)
生命科学顾问
617-435-6602
jallaire@lifesciadvisors.com

Alex Gray (investors)
Jasper Therapeutics
650-549-1454
agray@jaspertherapeutics.com

亚历克斯·格雷(投资者)
贾斯珀疗法
650-549-1454
agray@jaspertherapeutics.com

Lauren Walker (media)
Real Chemistry
646-564-2156
lbarbiero@realchemistry.com

劳伦·沃克(媒体)
真正的化学
646-564-2156
lbarbiero@realchemistry.com

译文内容由第三方软件翻译。


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