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临床试验/NCT03724851
NCT03724851已完成1 期

A Phase 1b/2a, Open-label, Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of Vactosertib in Combination with Pembrolizumab in Patients with Metastatic or Locally Advanced Colorectal or Gastric Cancer/ Gastroesophageal Junction Adenocarcinoma

MedPacto, Inc.5 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2018年12月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
120
试验地点
5
主要终点
Safety and Tolerability

研究概览

简要总结

This is an open-label, multicenter study to assess the safety, tolerability, pharmacokinetics, and antitumor activity of vactosertib in combination with pembrolizumab in patients with metastatic or locally advanced colorectal or gastric/gastroesophageal junction adenocarcinoma

详细描述

This is phase 1b/2a, open label, multi-center study to assess safety, tolerability, pharmacokinetics and anti-tumor activity of vactosertib in combination with pembrolizumab in patients with mCRC including CMS4 or diffuse GC/GEJC with two phases (Dose Finding Phase and Dose Expansion Phase). At screening, CMS4 will be classified by an experienced pathologist in the central lab that will examine the histology of primary surgical tissues. Approximately, 67 total patients are expected to be enrolled in this study. The first phase of the study, the Dose Finding Phase, will determine the MTD of the combination regimen. The second phase, the Dose Expansion Phase, will further evaluate the combination regimen to confirm RP2D.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Dose Expansion (300mg BID)

Experimental

TEW-7197 300mg BID, 5D/W + Pembrolizumab 200mg Q3W (n= 30)

干预措施: TEW-7197 (Drug)

Dose Expansion (200mg BID)

Experimental

TEW-7197 200mg BID, 5D/W + Pembrolizumab 200mg Q3W (n= 30)

干预措施: TEW-7197 (Drug)

Dose Expansion (200mg QD)

Experimental

TEW-7197 200mg QD, 5D/W + Pembrolizumab 200mg Q3W (n= 30)

干预措施: TEW-7197 (Drug)

结局指标

主要结局

Safety and Tolerability

时间窗: approximately 2 years

Incidence, nature and severity of adverse events (AEs) graded according to NCI CTCAE v5.0

Maximum Tolerated Dose

时间窗: approximately 2 years

Incidence of nature of DLTs

次要结局

  • Efficacy 3(up to 3 years)
  • Efficacy 1(approximately 2 years)
  • Efficacy 2(approximately 2 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (5)

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