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临床试验/NL-OMON56305
NL-OMON56305招募中不适用

A PHASE Ia/Ib DOSE-ESCALATION AND DOSE EXPANSION STUDY EVALUATING THE SAFETY, PHARMACOKINETICS, AND ACTIVITY OF GDC-6036 AS A SINGLE AGENT AND IN COMBINATION WITH OTHER ANTI-CANCER THERAPIES IN PATIENTS WITH ADVANCED OR METASTATIC SOLID TUMORS WITH A KRAS G12C MUTATION - GO42144

Genentech Inc. (een lid van de Roche groep)0 个研究点目标入组 15 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
15

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 documented advanced or metastatic solid tumor with KRAS G12C
  • mutation • Age > 18 years at time of signing Informed Consent Form • Women
  • of childbearing potential must agree to remain abstinent or use contraception,
  • and agree to refrain from donating eggs during the treatment period and after
  • the final dose of study as specified in the protocol • Men who are not
  • surgically sterile must agree to remain abstinent or use contraception, and
  • agreement to refrain from donating sperm during the treatment period and after
  • the final dose of study treatment as specified in the protocol

排除标准

  • Malabsorption or other condition that interferes with enteral absorption
  • Active brain metastases
  • Clinically significant cardiovascular dysfunction or liver disease

研究者

发起方
Genentech Inc. (een lid van de Roche groep)

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A PHASE Ia/Ib DOSE-ESCALATION AND DOSE EXPANSION... | 临床试验