jRCT2041250172招募中不适用
A Randomized, Double-Blind, Phase 3 Trial of Adagrasib plus Pembrolizumab plus Chemotherapy vs. Placebo plus Pembrolizumab plus Chemotherapy in Participants with Previously Untreated,Locally Advancedor Metastatic Non-squamous Non-small Cell Lung Cancer with KRASG12C Mutation(KRYSTAL-4) (KRYSTAL-4)
未提供0 个研究点目标入组 20 人开始时间: 待定
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 20
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
入排标准
- 年龄范围
- 18age old over 至 No limit(—)
- 性别
- All
入选标准
- •>Histologically or cytologically confirmed diagnosis of non-squamous NSCLC with evidence of KRAS G12C mutation via tumor sample and/or circulating tumor deoxyribonucleic acid (ctDNA).
- •>Locally advanced or metastatic disease.
- •>Measurable disease via computed tomography (CT) or magnetic resonance imaging (MRI) per RECIST v1.1 criteria of at least 1 lesion.
- •>No prior systemic anti-cancer therapy given for advanced or metastatic disease.
- •>Not a candidate for definitive therapy (eg, chemoradiation or complete surgical resection).
- •>Participants with brain metastases are eligible for enrollment, including those with untreated brain metastases. Brain metastases must be asymptomatic and not in need of immediate local therapy. Any untreated brain metastases must be <= 20 mm in diameter.
- •>Any PD-L1 expression (0 to 100%) as determined by VENTANA PD-L1 (SP263) assay, Agilent PD-L1 IHC 22C3 pharmDx, or Agilent PD-L1 IHC 28-8 pharmDx.
排除标准
- •>Participants with an active autoimmune or inflammatory disease requiring systemic treatment within 2 years.
- •>Uncontrolled or significant cardiovascular conditions within 6 months prior to enrollment that are ongoing or with risk of recurrence.
- •>Inadequate bone marrow or liver function or electrocardiogram (ECG) abnormalities.
- •>Ongoing treatment with concomitant medication known to cause prolonged QTc interval and that cannot be switched to alternative treatment prior to study entry.
- •>Treatment targeting KRAS G12C mutation (eg, sotorasib, adagrasib) in any setting.
- •>Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or study drug administration.
- •>Other protocol-defined Inclusion/Exclusion criteria apply.
研究者
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