Actively Recruiting

Phase 2
Age: 18Years - 75Years
All Genders
NCT05960955

Cadonilimab Combination With Chemotherapy With or Without AK117 in Resectable Gastric or Gastroesophageal Junction Adenocarcinoma

Led by Akeso · Updated on 2023-11-18

90

Participants Needed

1

Research Sites

211 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This trial is a Phase II study. All patients are resectable Gastric or Gastroesophageal Junction Adenocarcinoma, Eastern Cooperative Oncology Group (ECOG) performance status 0-1.The purpose of this study is to evaluate the efficacy and safety of cadonilimab combined with chemotherapy with or without AK117 neoadjuvantin treatment of resectable Gastric or Gastroesophageal Junction Adenocarcinoma.

CONDITIONS

Official Title

Cadonilimab Combination With Chemotherapy With or Without AK117 in Resectable Gastric or Gastroesophageal Junction Adenocarcinoma

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able and willing to provide written informed consent
  • Age between 18 and 75 years
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Histologically confirmed Gastric or Gastroesophageal Junction Adenocarcinoma
  • Stage T3-4N+M0 Gastric or Gastroesophageal Junction Adenocarcinoma (AJCC)
  • Measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1
  • Adequate organ function
Not Eligible

You will not qualify if you...

  • Suspected metastases or locally advanced, unresectable disease
  • Currently participating in a study of an investigational agent or using an investigational device
  • Major surgery within 30 days before Study Day 1
  • Active autoimmune disease requiring systemic treatment in the past 2 years
  • Known active Hepatitis B or Hepatitis C infection
  • History of myocardial infarction, unstable angina, or congestive heart failure within 12 months prior to study treatment
  • Known psychiatric or substance abuse disorders interfering with study cooperation
  • Received live virus vaccine within 30 days before planned first dose of study therapy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Tianjin Provincial Tumor Hospital

Tianjin, China

Actively Recruiting

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Research Team

W

Weifeng Song, MD

CONTACT

H

Han Liang, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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