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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 申请,要求评估 Claudin 6 阳性癌症中的 CTIM-76
GlobeNewswire ·  04/01 07:30

Important Regulatory Milestone Supports Next Phase of CTIM-76 Development

重要的监管里程碑支持 CTIM-76 开发的下一阶段

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.

费城,2024年4月1日(环球新闻专线)——推进实体瘤药物的生物制药公司Context Therapeutics Inc.(“Context” 或 “公司”)(纳斯达克股票代码:CNTX)今天宣布,该公司于2024年3月28日向美国食品药品监督管理局提交了研究性新药(IND)申请,以开始对 CTIM-76 的首次人体临床研究。IND 支持在克劳丁 6 (CLDN6) 阳性妇科和睾丸癌患者中启动 CTIM-76 的 1 期剂量递增和扩大临床试验。

"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首席执行官马丁·莱尔表示:“我们提交的 CTIM-76 IND 申请对Context来说是一个重要的里程碑。”“2021 年,我们设定了将 CTIM-76 推向临床的积极时间表,我们将该计划列为优先事项,因为我们认为它可能是一类最佳的 CLDN6 靶向疗法,对 CLDN6 具有高度选择性。IND 应用包括大量的制造、临床前和毒理学数据,以支持首次人体试验。我为整个 Context 团队为完成这份 IND 提交的不懈努力感到非常自豪。我们很高兴能继续推进 CTIM-76 的开发,并继续专注于为 1 期临床试验的启动做准备,以便我们能够尽快向医生及其患者提供 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.

关于 CTIM-76
CTIM-76 是一种具有双特异性抗体的 CLDN6 x CD3 T 细胞。CLDN6 富含多种实体瘤,包括卵巢、子宫内膜、肺、胃和睾丸。临床前研究表明,有可能以较低的免疫原性风险和可扩展的制造方式来满足大量可能有资格接受 CTIM-76 治疗的患者。

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.

关于上下文疗法
Context Therapeutics Inc.(纳斯达克股票代码:CNTX)是一家开发实体瘤药物的生物制药公司。Context正在开发 CTIM-76,这是一种针对CLDN6阳性肿瘤的选择性的 CLDN6 x CD3双特异性抗体,目前正在临床前开发中。CLDN6 是一种在多种实体瘤中表达的紧密连接膜蛋白靶标,包括卵巢、子宫内膜、睾丸和肺部,在健康的成人组织中不存在或低水平表达。Context 总部位于费城。欲了解更多信息,请在 X(前身为 Twitter)和 LinkedIn 上访问或关注本公司。

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.

前瞻性陈述
本新闻稿包含 “前瞻性陈述”,这些陈述涉及重大风险和不确定性,以实现1995年《私人证券诉讼改革法》提供的安全港。除历史事实陈述外,本新闻稿中有关管理层战略、未来运营、前景、计划和目标的任何陈述,包括 “可能”、“将”、“期望”、“预期”、“展望”、“展望”、“计划”、“打算” 和类似表述(以及其他提及未来事件、条件或情况的词语或表述)均为前瞻性陈述。其中包括但不限于以下方面的声明:(i) 我们预计启动 CTIM-76 的 1 期试验以及参与此类试验的适应症,(ii) 我们对任何 CTIM-76 试验试验设计的期望,(iii) 我们对 CTIM-76 IND 中数据质量的信念,(iv) 我们期望获得 FDA 的 CTIM-76 的临床许可,(v) CTIM-76 的潜在益处、特征、安全性和副作用概况,(vi) CTIM-76 具有益处、特征和副作用特征的能力与第三方候选产品有区别和/或更好,(vii)可能性数据支持 CTIM-76 的未来开发,以及(viii)CTIM-76 获得监管部门批准的可能性。本新闻稿中的前瞻性陈述涉及重大风险和不确定性,可能导致实际结果与前瞻性陈述所表达或暗示的结果存在重大差异,因此我们无法向您保证我们的计划、意图、预期或战略将实现或实现。我们向美国证券交易委员会提交的文件中讨论了可能导致实际业绩与本新闻稿中前瞻性陈述中表达或暗示的结果不同的其他因素,包括其中包含的 “风险因素” 部分。除非法律另有要求,否则我们不打算或义务更新或修改任何前瞻性陈述,这些陈述仅代表其发表之日,无论是由于新信息、未来事件、情况还是其他原因。

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

媒体联系人:
吉娜·曼贾拉西娜
6 度
917-797-7904
gmangiaracina@6degreespr.com

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

投资者关系联系人:
詹妮弗·米奈-阿扎里
上下文疗法
IR@contexttherapeutics.com


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