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Context Therapeutics Submits IND Application to Evaluate CTIM-76 in Claudin 6-Positive Cancers

Context Therapeutics Submits IND Application to Evaluate CTIM-76 in Claudin 6-Positive Cancers

Context Therapeutics 提交了 IND 申請,要求評估 Claudin 6 陽性癌症中的 CTIM-76
GlobeNewswire ·  04/01 19:30

Important Regulatory Milestone Supports Next Phase of CTIM-76 Development

重要的監管里程碑支持 CTIM-76 開發的下一階段

PHILADELPHIA, April 01, 2024 (GLOBE NEWSWIRE) -- Context Therapeutics Inc. ("Context" or the "Company") (Nasdaq: CNTX), a biopharmaceutical company advancing medicines for solid tumors, today announced that on March 28, 2024, the Company submitted an Investigational New Drug (IND) application to the U.S. Food and Drug Administration to begin a first-in-human clinical study of CTIM-76. The IND supports the initiation of a Phase 1 dose escalation and expansion clinical trial of CTIM-76 in patients with Claudin 6 (CLDN6)-positive gynecologic and testicular cancers.

費城,2024年4月1日(環球新聞專線)——推進實體瘤藥物的生物製藥公司Context Therapeutics Inc.(“Context” 或 “公司”)(納斯達克股票代碼:CNTX)今天宣佈,該公司於2024年3月28日向美國食品藥品監督管理局提交了研究性新藥(IND)申請,以開始對 CTIM-76 的首次人體臨床研究。IND 支持在克勞丁 6 (CLDN6) 陽性婦科和****癌患者中啓動 CTIM-76 的 1 期劑量遞增和擴大臨床試驗。

"Our IND submission for CTIM-76 is a significant milestone for Context," said Martin Lehr, CEO of Context. "In 2021, we set an aggressive timeline to advance CTIM-76 into the clinic and we prioritized this program as we believe it is a potentially best-in-class CLDN6-targeting therapy that is highly selective for CLDN6. The IND application includes extensive manufacturing, preclinical, and toxicology data to support a first-in-human trial. I am incredibly proud of the entire Context team who worked tirelessly to complete this IND submission. We are excited to continue advancing the development of CTIM-76 and remain focused on preparing for the initiation of the Phase 1 clinical trial so that we can make CTIM-76 available to physicians and their patients as soon as possible."

Context首席執行官馬丁·萊爾表示:“我們提交的 CTIM-76 IND 申請對Context來說是一個重要的里程碑。”“2021 年,我們設定了將 CTIM-76 推向臨床的積極時間表,我們將該計劃列爲優先事項,因爲我們認爲它可能是一類最佳的 CLDN6 靶向療法,對 CLDN6 具有高度選擇性。IND 應用包括大量的製造、臨床前和毒理學數據,以支持首次人體試驗。我爲整個 Context 團隊爲完成這份 IND 提交的不懈努力感到非常自豪。我們很高興能繼續推進 CTIM-76 的開發,並繼續專注於爲 1 期臨床試驗的啓動做準備,以便我們能夠儘快向醫生及其患者提供 CTIM-76。”

About CTIM-76
CTIM-76 is a CLDN6 x CD3 T cell engaging bispecific antibody. CLDN6 is enriched in a wide range of solid tumors, including ovarian, endometrial, lung, gastric, and testicular. Preclinical research suggests the potential for convenient dosing with low immunogenicity risk and scalable manufacturing to address the significant number of patients who are potentially eligible for CTIM-76 therapy.

關於 CTIM-76
CTIM-76 是一種具有雙特異性抗體的 CLDN6 x CD3 T 細胞。CLDN6 富含多種實體瘤,包括卵巢、子宮內膜、肺、胃和****。臨床前研究表明,有可能以較低的免疫原性風險和可擴展的製造方式來滿足大量可能有資格接受 CTIM-76 治療的患者。

About Context Therapeutics
Context Therapeutics Inc. (Nasdaq: CNTX) is a biopharmaceutical company advancing medicines for solid tumors. Context is developing CTIM-76, a selective CLDN6 x CD3 bispecific antibody for CLDN6-positive tumors, currently in preclinical development. CLDN6 is a tight junction membrane protein target expressed in multiple solid tumors, including ovarian, endometrial, testicular, and lung, and absent from or expressed at low levels in healthy adult tissues. Context is headquartered in Philadelphia. For more information, please visit or follow the Company on X (formerly Twitter) and LinkedIn.

關於上下文療法
Context Therapeutics Inc.(納斯達克股票代碼:CNTX)是一家開發實體瘤藥物的生物製藥公司。Context正在開發 CTIM-76,這是一種針對CLDN6陽性腫瘤的選擇性的 CLDN6 x CD3雙特異性抗體,目前正在臨床前開發中。CLDN6 是一種在多種實體瘤中表達的緊密連接膜蛋白靶標,包括卵巢、子宮內膜、****和肺部,在健康的成人組織中不存在或低水平表達。Context 總部位於費城。欲了解更多信息,請在 X(前身爲 Twitter)和 LinkedIn 上訪問或關注本公司。

Forward-looking Statements
This press release contains "forward-looking statements" that involve substantial risks and uncertainties for purposes of the safe harbor provided by the Private Securities Litigation Reform Act of 1995. Any statements, other than statements of historical fact, included in this press release regarding strategy, future operations, prospects, plans and objectives of management, including words such as "may," "will," "expect," "anticipate," "look forward," "plan," "intend," and similar expressions (as well as other words or expressions referencing future events, conditions, or circumstances) are forward-looking statements. These include, without limitation, statements regarding (i) our expectation to initiate a Phase 1 trial for CTIM-76 and the indications to be part of such trials, (ii) our expectation regarding the trial design of any CTIM-76 trial, (iii) our belief regarding the quality of the data included in our IND for CTIM-76, (iv) our expectation to receive IND clearance from the FDA for CTIM-76, (v) the potential benefits, characteristics, safety and side effect profile of CTIM-76, (vi) the ability of CTIM-76 to have benefits, characteristics, and a side effect profile that is differentiated and/or better than third party product candidates, (vii) the likelihood data will support future development of CTIM-76, and (viii) the likelihood of obtaining regulatory approval for CTIM-76. Forward-looking statements in this release involve substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by the forward-looking statements, and we therefore cannot assure you that our plans, intentions, expectations, or strategies will be attained or achieved. Other factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in our filings with the U.S. Securities and Exchange Commission, including the section titled "Risk Factors" contained therein. Except as otherwise required by law, we disclaim any intention or obligation to update or revise any forward-looking statements, which speak only as of the date they were made, whether as a result of new information, future events, or circumstances or otherwise.

前瞻性陳述
本新聞稿包含 “前瞻性陳述”,這些陳述涉及重大風險和不確定性,以實現1995年《私人證券訴訟改革法》提供的安全港。除歷史事實陳述外,本新聞稿中有關管理層戰略、未來運營、前景、計劃和目標的任何陳述,包括 “可能”、“將”、“期望”、“預期”、“展望”、“展望”、“計劃”、“打算” 和類似表述(以及其他提及未來事件、條件或情況的詞語或表述)均爲前瞻性陳述。其中包括但不限於以下方面的聲明:(i) 我們預計啓動 CTIM-76 的 1 期試驗以及參與此類試驗的適應症,(ii) 我們對任何 CTIM-76 試驗試驗設計的期望,(iii) 我們對 CTIM-76 IND 中數據質量的信念,(iv) 我們期望獲得 FDA 的 CTIM-76 的臨床許可,(v) CTIM-76 的潛在益處、特徵、安全性和副作用概況,(vi) CTIM-76 具有益處、特徵和副作用特徵的能力與第三方候選產品有區別和/或更好,(vii)可能性數據支持 CTIM-76 的未來開發,以及(viii)CTIM-76 獲得監管部門批准的可能性。本新聞稿中的前瞻性陳述涉及重大風險和不確定性,可能導致實際結果與前瞻性陳述所表達或暗示的結果存在重大差異,因此我們無法向您保證我們的計劃、意圖、預期或戰略將實現或實現。我們向美國證券交易委員會提交的文件中討論了可能導致實際業績與本新聞稿中前瞻性陳述中表達或暗示的結果不同的其他因素,包括其中包含的 “風險因素” 部分。除非法律另有要求,否則我們不打算或義務更新或修改任何前瞻性陳述,這些陳述僅代表其發表之日,無論是由於新信息、未來事件、情況還是其他原因。

Media Contact:
Gina Mangiaracina
6 Degrees
917-797-7904
gmangiaracina@6degreespr.com

媒體聯繫人:
吉娜·曼賈拉西娜
6 度
917-797-7904
gmangiaracina@6degreespr.com

Investor Relations Contact:
Jennifer Minai-Azary
Context Therapeutics
IR@contexttherapeutics.com

投資者關係聯繫人:
詹妮弗·米奈-阿扎裏
上下文療法
IR@contexttherapeutics.com


譯文內容由第三人軟體翻譯。


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