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Not yet recruiting Phase 3 Interventional

Phase 3 Study of Cadonilimab Combined With Chemotherapy vs Chemotherapy in Combination With or Without Nivolumab for the 1L Treatment of Participants With HER2-negative, Previously Untreated, Unresectable or Metastatic Gastric/GEJ Adenocarcinoma

ClinicalTrials.gov ID: NCT07700979

Public ClinicalTrials.gov record NCT07700979. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:32 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Multi-regional Phase 3 Study of Cadonilimab Combined With Chemotherapy Versus Chemotherapy in Combination With or Without Nivolumab for the First-line Treatment of Participants With HER2-negative, Previously Untreated, Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma

Study identification

NCT ID
NCT07700979
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Akeso
Industry
Enrollment
900 participants

Conditions and interventions

Interventions

  • Cadonilimab Drug
  • CAPOX regimen Drug
  • Nivolumab Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 19, 2026
Primary completion
Aug 17, 2029
Completion
Aug 17, 2030
Last update posted
Jul 13, 2026

2026 – 2030

United States locations

U.S. sites
13
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Mayo Clinic Phoenix Arizona 85054
UCLA Health Los Angeles California 90095
Rocky Mountain Cancer Centers Denver Colorado 80218
Yale School of Medicine New Haven Connecticut 06510
Dana Farber Cancer Institute Boston Massachusetts 02215
Henry Ford Health Detroit Michigan 48202
Mount Sinai New York New York 10029
Memorial Sloan Kettering Cancer Center New York New York 10065
Oregon Health and Science University Portland Oregon 97239
Sarah Cannon Research Institute (SCRI) - Oncology Partners Nashville Tennessee 37203
Baylor Scott & White Health Dallas Texas 75246
MD Anderson Cancer Center Houston Texas 77030
University of Wisconsin Carbone Cancer Center Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07700979, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 13, 2026 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07700979 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →