Trial intelligence / Profile preview

Sintilimab and Bevacizumab with Chemotherapy for Peritoneal Mesothelioma

NCT06543069Phase 2

Key facts

Status
Recruiting
Start
Jan 2024
Primary completion
Jan 2026
Countries
1
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Modality
Monoclonal Antibodies
Conditions
malignant peritoneal mesothelioma (MPM)
01

Overview

Phase 2, open-label, single-arm trial of sintilimab and bevacizumab in malignant peritoneal mesothelioma (MPM), sponsored by Cancer Institute and Hospital, Chinese Academy of Medical Sciences. Primary endpoint: Progression-Free Survival at 36 months. Started Jan 2024; status: recruiting.

02

Design

1 arm
Study design
Non-randomizedOpen-labelSingle group
  • Single Arm

    Sintilimab + Bevacizumab + Pemetrexed + Cisplatin

03

Who it enrols

Adult patients with pathologically confirmed unresectable malignant peritoneal mesothelioma, ECOG 0-1, and adequate organ function. Excludes patients with active autoimmune diseases, significant cardiovascular disease, or recent bleeding tendencies.

04

Endpoints

Primary

  • Progression-Free Survival

Secondary

  • Overall Survival

  • Objective Response Rate

  • Disease Control Rate

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