跳至主要内容
临床试验/CTIS2022-502031-20-00
CTIS2022-502031-20-00招募中1 期

A Phase II/III, Randomized, Double-Blind, Placebo-Controlled Study of Tiragolumab in combination with Atezolizumab plus Pemetrexed and Carboplatin/Cisplatin versus Pembrolizumab plus Pemetrexed and Carboplatin/Cisplatin in Patients with previously Untreated Advanced Non-Squamous Non-Small-Cell Lung Cancer - BO42592

F. Hoffmann-La Roche AG0 个研究点目标入组 500 人开始时间: 2024年5月9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
500

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

  • 1. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1, 2. Histologically or cytologically documented locally advanced unresectable or metastatic non-squamous NSCLC that is not eligible for curative surgery and/or definitive chemoradiotherapy, 3. No prior systemic treatment for metastatic non-squamous NSCLC, 4. Known tumor PD-L1 status, 5. Measurable disease, as defined by RECIST v1.1, 6.Negative HIV test and Serology test negative for active hepatitis B virus and active hepatitis C virus at screening

排除标准

  • 1. Patients with NSCLC which harbors a mutation in the EGFR gene or an ALK fusion oncogene, 2. Symptomatic, untreated, or actively progressing central nervous system (CNS) metastases, 3. Active or history of autoimmune disease or immune deficiency, 4. History of idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis, 5. History of malignancy other than NSCLC within 5 years prior to randomization, with the exception of malignancies with a negligible risk of metastasis or death, 6. Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including anti-cytotoxic T lymphocyte-associated protein 4 (CTLA4), anti-TIGIT, anti-PD-1, and anti-PD-L1 therapeutic antibodies

研究者

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