ClinicalTrials.gov record
Withdrawn Phase 2 Interventional

An Investigational Immuno-therapy Study of Relatlimab Plus Nivolumab Compared to Various Standard-of-Care Therapies in Previously Treated Participants With Recurrent, Advanced or Metastatic Gastric Cancer or Gastroesophageal Junction Adenocarcinoma

ClinicalTrials.gov ID: NCT03704077

Public ClinicalTrials.gov record NCT03704077. 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 May 18, 2026, 5:26 AM 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, Active-Controlled, Open-Label, Phase 2 Clinical Trial of BMS-986213, in Combination With Various Standard-of-Care Therapeutic Regimens, in Participants With Recurrent, Locally Advanced, or Metastatic Gastric Cancer (GC) or Gastroesophageal Junction (GEJ) Adenocarcinoma

Study identification

NCT ID
NCT03704077
Recruitment status
Withdrawn
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • Nivolumab Biological
  • Paclitaxel Drug
  • Ramucirumab Drug
  • Relatlimab + Nivolumab Biological

Biological · 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
Oct 30, 2019
Primary completion
Feb 26, 2022
Completion
Sep 29, 2024
Last update posted
May 18, 2020

2019 – 2024

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Local Institution Daphne Alabama 36526
Local Institution Bakersfield California 93309
Local Institution Fullerton California 92835
Local Institution Los Angeles California 90095
Local Institution Redondo Beach California 90277
Local Institution Santa Barbara California 93105
Local Institution Aurora Colorado 80045
Local Institution Lakewood Colorado 80228
Local Institution Miami Florida 33176
Local Institution Tampa Florida 33612
Local Institution Marietta Georgia 30060
Local Institution Boston Massachusetts 02215
Local Institution St Louis Missouri 63110
Local Institution New Brunswick New Jersey 08009
Local Institution Chapel Hill North Carolina 27599
Local Institution Charlotte North Carolina 28204
Local Institution Fargo North Dakota 58102
Local Institution Allentown Pennsylvania 18103
Local Institution Sioux Falls South Dakota 57104
Local Institution Vancouver Washington 98684

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 64 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03704077, 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 May 18, 2020 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03704077 live on ClinicalTrials.gov.

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