跳至主要内容
临床试验/NL-OMON43272
NL-OMON43272已完成不适用

A Phase 1/2 Multicenter Study of BMS-986012 in Subjects with Relapsed / Refractory Small Cell Lung Cancer (CA001-030) - CA001-030 BMS-986012 in Relapsed / Refractory Small Cell Lung Cancer

Bristol-Myers Squibb0 个研究点目标入组 6 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
已完成
发起方
入组人数
6

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

  • - Signed Written Informed Consent
  • - Men and women at least 18 years of age with histological or cytological confirmed pulmonary SCLC
  • - Have relapsed after or are refractory to first line therapy and have not yet received two
  • or more lines of anticancer treatment
  • - Last exposure to anticancer therapy within 4 weeks or 5 half-lives (whichever is longer) prior to study drug administration
  • - At least one measurable lesion per RECIST v1.1
  • - Adequate organ function
  • - Comply with visit and treatment schedule, sample collection for laboratory tests, and treatment and follow-up

排除标准

  • - Known or suspected brain metastasis
  • - Non-pulmonary small cell cancer
  • - Acute or chronic medical illness
  • - Uncontrolled or significant cardiac disease
  • - Infection requiring systemic treatment
  • - Grade 2 or higher peripheral neuropathy
  • - Other concomitant malignancies (except unless complete remission was achieved 3 yrs prior to study entry)
  • - HIV-related disease, HIV+, HepB, HepC
  • - Allergies or adverse drug reaction

研究者

发起方
Bristol-Myers Squibb

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