跳至主要内容
临床试验/CTIS2023-503868-16-00
CTIS2023-503868-16-00招募中1 期

A Phase III, Randomized, Open-Label, Multicenter Study of Lurbinectedin in Combination with Atezolizumab Compared with Atezolizumab as Maintenance Therapy in Participants with Extensive-Stage Small-Cell Lung Cancer (ES-SCLC) Following First-Line Induction Therapy with Carboplatin, Etoposide and Atezolizumab - GO43104

F. Hoffmann-La Roche AG0 个研究点目标入组 658 人开始时间: 2024年5月31日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
658

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Histologically or cytologically confirmed ES-SCLC (per the VALG staging system), Adequate hematologic and end-organ function, ECOG PS 0 or 1, No prior systemic treatment for ES-SCLC, Ongoing response or stable disease per RECIST v1.1 after completion of the induction therapy, Toxicities attributed to prior induction anti-cancer therapy or PCI resolved to Grade 1 or better

排除标准

  • Presence or history of CNS metastases, Planned consolidative chest radiation, Uncontrolled pleural effusion, pericardial effusion or ascites requiring recurrent drainage procedures, Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including anti-CTLA-4, anti-PD-1, and anti-PD-L1 therapeutic antibodies, or lurbinectedin or trabectedin, History of idiopathic pulmonary fibrosis, organizing pneumonia, drug induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest computed tomography (CT) scan, Disease progression following induction treatment

研究者

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