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临床试验/NL-OMON53747
NL-OMON53747招募中不适用

A PHASE Ib/II, OPEN-LABEL, MULTICENTER STUDY EVALUATING THE SAFETY, ACTIVITY, AND PHARMACOKINETICS OF GDC-6036 IN COMBINATION WITH OTHER ANTI-CANCER THERAPIES IN PATIENTS WITH PREVIOUSLY UNTREATED ADVANCED OR METASTATIC NON-SMALL CELL LUNG CANCER WITH A KRAS G12C MUTATION - BO44426 - GDC-6036- NSCLC KRAS

Roche Nederland B.V.0 个研究点目标入组 5 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
5

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 99(—)

入选标准

  • - Histologically or cytologically documented locally advanced unresectable or
  • metastatic NSCLC that is not eligible for curative surgery and/or definitive
  • chemoradiotherapy
  • - No prior systemic treatment for advanced unresectable or metastatic NSCLC
  • - Confirmation of Biomarker eligibility:
  • .. Documented history of the KRAS G12C mutation
  • .. Documented history of PD-L1 tumor cell expression >=1%
  • - Pre-treatment tumor tissue along with an associated pathology report is
  • required for all participants enrolled on study. Representative tumor
  • specimens must be in formalin*fixed, paraffin embedded (FFPE) blocks
  • (preferred) or 15 unstained, freshly cut, serial slides. Although 15 slides
  • are required, if only 10 slides are available, the participant may be eligible
  • for the study following consultation with the Sponsor
  • - Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1
  • - Measurable disease, as defined by Response Evaluation Criteria in Solid
  • Tumors (RECIST) v1.1

排除标准

  • - Known concomitant second oncogenic driver with available targeted treatment
  • - Symptomatic, untreated, or actively progressing central nervous system (CNS)
  • - Prior treatment with a KRAS G12C inhibitor
  • - Known hypersensitivity to any of the components of GDC-6036 or pembrolizumab
  • - History of malignancy other than NSCLC within 5 years prior to initiation of
  • study treatment, with the exception of malignancies with a negligible risk of
  • metastasis or death (e.g., 5-year OS rate more >90%), such as adequately
  • treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, localized
  • prostate cancer, ductal breast carcinoma in situ, or Stage I uterine cancer
  • - Uncontrolled tumor related pain, pleural effusion, pericardial effusion, or
  • ascites requiring recurrent drainage procedures, uncontrolled or symptomatic
  • hypercalcemia
  • - History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g.,
  • bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis,
  • or evidence of active pneumonitis, active tuberculosis, significant
  • cardiovascular disease within 3 months prior to initiation of study treatment

研究者

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