BENITIONSClinical Trial Intelligence

Study Evaluating Tarlatamab in Chinese Participants With Advanced Small Cell Lung Cancer After Two or More Prior Lines of Treatment

2期 进行中(已停止招募) NCT06502977

适应症Extensive Stage Small Cell Lung Cancer
分期2期
申办方Amgen
状态进行中(已停止招募)
受试者人数32 人
干预(药物)Tarlatamab
开始日期2024年8月27日
完成日期2025年3月28日
结果公布日2026年4月15日

摘要

The primary aim of this study is to evaluate the efficacy of tarlatamab as assessed by objective response rate (ORR) based on blinded independent central review (BICR) per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1).

Objective Response Rate (ORR) Based on Blinded Independent Central Review (BICR) Per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1)

From first dose of trial drug up to a minimum of last dose + 65 days or data cutoff date; median (min, max) time on trial was 3.4 (2.2, 6.5) months at data cut off · percentage of participants

Tarlatamab38.7 percentage of participants

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。