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8-K: Current report

8-K: Current report

8-K:重大事件
美股SEC公告 ·  05/20 08:40
Moomoo AI 已提取核心信息
On May 20, 2024, eFFECTOR Therapeutics, Inc. announced a collaboration with the Dana-Farber Cancer Institute to conduct a Phase 2 investigator-sponsored trial (IST) for evaluating the combination of zotatifin, abemaciclib, and letrozole in treating patients with estrogen receptor-positive endometrial cancer and low grade serous ovarian cancer. The trial aims to overcome resistance to CDK4/6 inhibition by targeting eIF4A to downregulate factors implicated in resistance, potentially enhancing therapeutic benefits. The company's forward-looking statements indicate belief in the potential benefits and successful future development of their product candidates, while acknowledging the risks and uncertainties inherent in clinical trials and regulatory processes.
On May 20, 2024, eFFECTOR Therapeutics, Inc. announced a collaboration with the Dana-Farber Cancer Institute to conduct a Phase 2 investigator-sponsored trial (IST) for evaluating the combination of zotatifin, abemaciclib, and letrozole in treating patients with estrogen receptor-positive endometrial cancer and low grade serous ovarian cancer. The trial aims to overcome resistance to CDK4/6 inhibition by targeting eIF4A to downregulate factors implicated in resistance, potentially enhancing therapeutic benefits. The company's forward-looking statements indicate belief in the potential benefits and successful future development of their product candidates, while acknowledging the risks and uncertainties inherent in clinical trials and regulatory processes.
2024年5月20日,Effector Therapeutics, Inc.宣布与达纳-法伯癌症研究所合作进行一项由研究者赞助的2期试验(IST),评估佐他替芬、阿贝马西利布和来曲唑联合治疗雌激素受体阳性子宫内膜癌和低度浆液性卵巢癌患者的情况。该试验旨在通过靶向EIF4a来下调与耐药性有关的因素,从而克服对CDK4/6抑制的耐药性,从而有可能提高治疗益处。该公司的前瞻性陈述表明,他们相信其候选产品的潜在收益和未来的成功开发,同时承认临床试验和监管程序中固有的风险和不确定性。
2024年5月20日,Effector Therapeutics, Inc.宣布与达纳-法伯癌症研究所合作进行一项由研究者赞助的2期试验(IST),评估佐他替芬、阿贝马西利布和来曲唑联合治疗雌激素受体阳性子宫内膜癌和低度浆液性卵巢癌患者的情况。该试验旨在通过靶向EIF4a来下调与耐药性有关的因素,从而克服对CDK4/6抑制的耐药性,从而有可能提高治疗益处。该公司的前瞻性陈述表明,他们相信其候选产品的潜在收益和未来的成功开发,同时承认临床试验和监管程序中固有的风险和不确定性。
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