跳至主要内容
临床试验/NL-OMON56429
NL-OMON56429招募中不适用

A Phase 1a/1b Open label, Multicenter, Global, Dose-Escalation Study to Evaluate the Safety and Pharmacokinetics of XMAB24306 as a Single Agent and in Combination with Atezolizumab in Patients with Locally Advanced or Metastatic Solid Tumors - GO41596

Genentech Inc. (een lid van de Roche Group)0 个研究点目标入组 32 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
32

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

  • Age >= 18 years at time of signing Informed Consent Form
  • ECOG Performance Status of 0 or 1
  • Life expectancy >= 12 weeks
  • Adequate hematologic and end-organ function
  • For patients receiving therapeutic anticoagulation: stable anticoagulant
  • Negative serum pregnancy test for women of childbearing potential: agreement
  • to remain abstinent (refrain from heterosexual intercourse) or use contraception
  • For men: agreement to remain abstinent (refrain from heterosexual
  • intercourse) or use a condom
  • Histologically confirmed locally advanced, recurrent, or metastatic incurable
  • solid tumor malignancy
  • Measurable disease per RECIST v1.1

排除标准

  • Pregnant or breastfeeding, or intending to become pregnant during the study
  • Significant cardiovascular disease
  • Current treatment with medications that prolong the QT interval
  • Known clinically significant liver disease
  • Poorly controlled Type 2 diabetes mellitus
  • Symptomatic, untreated, or actively progressing CNS metastases
  • History of leptomeningeal disease
  • History of malignancy other than disease under study within 3 years prior to
  • Active or history of autoimmune disease or immune deficiency
  • Active tuberculosis, hepatitis B, hepatitis C, or known/suspected Epstein
  • Barr virus infection
  • Positive test for HIV infection
  • Prior allogeneic stem cell or solid organ transplantation

研究者

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

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