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Johnson & Johnson Announces RYBREVANT Plus LAZCLUZE Show Statistically Significant And Clinically Meaningful Improvement In Overall Survival Versus Osimertinib; Median Overall Survival Improvement Expected To Exceed One Year; First And Only Regimen...

Johnson & Johnson Announces RYBREVANT Plus LAZCLUZE Show Statistically Significant And Clinically Meaningful Improvement In Overall Survival Versus Osimertinib; Median Overall Survival Improvement Expected To Exceed One Year; First And Only Regimen...

强生宣布RYBREVANt和LAZCLUZE显示在总体生存期上与Osimertinib相比有统计学显著性和临床意义的改善;预计中位总体生存期的改善将超过一年;这是首个也是唯一的方案...
Benzinga ·  01/07 21:16

Johnson & Johnson Announces RYBREVANT Plus LAZCLUZE Show Statistically Significant And Clinically Meaningful Improvement In Overall Survival Versus Osimertinib; Median Overall Survival Improvement Expected To Exceed One Year; First And Only Regimen With A Survival Benefit Over Current Standard Of Care In First-line Treatment Of EGFR-Mutated Lung Cancer

强生宣布,与奥西替尼相比,Rybrevant Plus LAZCLUZE的总体存活率在统计学上显著且具有临床意义的改善;总体存活率中位数预计将超过一年;表皮生长因子突变肺癌一线治疗中第一个也是唯一一个存活率优于当前护理标准的方案

Median overall survival improvement expected to exceed one year

总体存活率改善中位数预计将超过一年

First and only regimen with a survival benefit over current standard of care in first-line treatment of EGFR-mutated lung cancer

在表皮生长因子突变肺癌的一线治疗中,第一种也是唯一一种比当前护理标准更具存活益处的方案

RARITAN, N.J., Jan. 7, 2025 /PRNewswire/ -- Johnson & Johnson (NYSE:JNJ) today announced positive topline results for the gold standard endpoint in cancer treatment of overall survival (OS) from the Phase 3 MARIPOSA study, evaluating RYBREVANT (amivantamab-vmjw) plus LAZCLUZE (lazertinib) as a first-line therapy for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletions (ex19del) or L858R substitution mutations. The chemotherapy-free combination regimen met the final pre-specified secondary endpoint of OS and demonstrated clinically meaningful and statistically significant improvement in OS versus the current standard of care osimertinib. Improvement in median OS is expected to exceed one year.

新泽西州拉里坦,2025年1月7日 /PRNewswire/ — 强生公司(纽约证券交易所代码:JNJ)今天宣布了MARIPOSA三期研究中癌症治疗总存活率(OS)的黄金标准终点结果为阳性,该研究评估了Rybrevant(amivantamab-vmjw)和LAZCLUZE(拉泽替尼)作为患者一线疗法局部晚期或转移性非小细胞肺癌 (NSCLC) 伴有表皮生长因子受体 (EGFR) 19 外显子缺失 (ex19del) 或 L858R 替代突变。该免化疗联合方案符合OS的最终预先规定的次要终点,与当前的标准奥美替尼相比,OSIMERTINIB显示出具有临床意义和统计学意义的改善。中位操作系统的改善预计将超过一年。

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