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Black Diamond Therapeutics 宣布 2 期初始数据显示 BDTX-1535 在具有广谱经典、非经典和 C797S 耐药突变的复发性 EGFRm NSCLC 患者中具有强大的抗肿瘤活性 --BDTX-1535 dose of 200 mg daily selected for pivotal development; favorable tolerability profile and no new safety signals observed --Preliminary ORR of 42% in 19 patients at 200 mg with on-target resistance EGFR mutations --1 9 例 200 mg 且靶向耐药 EGFR 突变患者的初步 ORR 为 42% --Encouraging durability with DOR of approximately 8 months or more for first 3 patients with a PR; 14 of 19 patients remain on treatment --Regulatory feedback on registration path anticipated in Q1 2025 --Initial results of BDTX-1535 in first-line NSCLC patients with non-classical EGFR mutations expected Q1 2025 马萨诸塞州剑桥,2024 年 9 月 23 日 (GLOBE NEWSWIRE) -- Black Diamond Therapeutics, Inc. (纳斯达克股票代码:BDTX)是一家临床阶段的肿瘤学公司,开发针对癌
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