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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03704077
Other study ID # CA224-061
Secondary ID 2018-001070-20
Status Withdrawn
Phase Phase 2
First received
Last updated
Start date October 31, 2019
Est. completion date September 30, 2024

Study information

Verified date May 2020
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effectiveness of relatlimab plus nivolumab, alone or in combination with various standard-of-care treatments in participants with gastric cancer (GC) or gastroesophageal junction (GEJ) adenocarcinoma that has come back or spread to other places in the body after prior therapy.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date September 30, 2024
Est. primary completion date February 27, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com

Inclusion Criteria:

- Histologically or cytologically confirmed locally advanced or recurrent or metastatic GC or GEJ adenocarcinoma that is considered incurable by local therapies such as radiation or surgery

- Evidence of progressive disease (PD) on at least one prior platinum- and fluoropyrimidine-containing chemotherapy regimen

- Available tumor tissue for biomarker analysis

Exclusion Criteria:

- Must not have squamous cell or undifferentiated GC or GEJ

- Untreated known central nervous system (CNS) metastases

- Uncontrolled or significant cardiovascular disease

Other protocol defined inclusion/exclusion criteria could apply

Study Design


Intervention

Biological:
Relatlimab + Nivolumab
Specified dose on specified days
Nivolumab
Specified dose on specified days
Drug:
Paclitaxel
Specified dose on specified days
Ramucirumab
Specified dose on specified days

Locations

Country Name City State
Argentina Local Institution Buenos Aires
Argentina Local Institution Caba
Argentina Local Institution Ciudad Autonoma de Buenos Aires
Argentina Local Institution Cordoba
Argentina Local Institution Viedma RIO Negro
Australia Local Institution Bedford Park
Australia Local Institution Heidelberg Victoria
Australia Local Institution Malvern Victoria
Australia Local Institution Melbourne Victoria
Australia Local Institution Murdoch
Australia Local Institution Westmead New South Wales
Brazil Local Institution Barretos SAO Paulo
Brazil Local Institution Belo Horizonte Minas Gerais
Brazil Local Institution Fortaleza Ceara
Brazil Local Institution Jau SAO Paulo
Brazil Local Institution Porto Alegre RIO Grande DO SUL
Brazil Local Institution Rio de Janeiro
Brazil Local Institution Sao Paulo
Canada Local Institution Halifax Nova Scotia
Canada Local Institution Hamilton Ontario
Canada Local Institution Montreal Quebec
Canada Local Institution Ottawa Ontario
Canada Local Institution Sherbrooke Quebec
Canada Local Institution Toronto Ontario
Canada Local Institution Toronto Ontario
Chile Local Institution Santiago Metropolitana
Chile Local Institution Santiago Metropolitana
Colombia Local Institution Medellin
Germany Local Institution Berlin
Germany Local Institution Cologne
Germany Local Institution Erlangen
Germany Local Institution Essen
Germany Local Institution Frankfurt am Main
Germany Local Institution Freiburg
Germany Local Institution Hamburg
Germany Local Institution Hannover
Germany Local Institution Jena
Germany Local Institution Mainz
Germany Local Institution Mannheim
Germany Local Institution Marburg
Germany Local Institution Paderborn
Germany Local Institution Reutlingen
Germany Local Institution Wiesbaden
Italy Local Institution Bergamo
Italy Local Institution Milano
Italy Local Institution Napoli
Italy Local Institution Reggio Emilia
Mexico Local Institution Aguascalientes
Mexico Local Institution Merida Yucatan
Mexico Local Institution Mexico City Distrito Federal
Mexico Local Institution Tuxtla Gutierrez Chiapas
Mexico Local Institution ZONA Centro. LEON Guanajuato
Portugal Local Institution Lisboa
Portugal Local Institution Porto
Puerto Rico Local Institution Rio Piedras
Romania Local Institution Bucuresti
Romania Local Institution Cluj-Napoca
Romania Local Institution Craiova
Romania Local Institution Floresti
Spain Local Institution Badajoz
Spain Local Institution Madrid
Spain Local Institution Madrid
Spain Local Institution Madrid
Spain Local Institution Valencia
United States Local Institution Allentown Pennsylvania
United States Local Institution Aurora Colorado
United States Local Institution Bakersfield California
United States Local Institution Boston Massachusetts
United States Local Institution Chapel Hill North Carolina
United States Local Institution Charlotte North Carolina
United States Local Institution Daphne Alabama
United States Local Institution Fargo North Dakota
United States Local Institution Fullerton California
United States Local Institution Lakewood Colorado
United States Local Institution Los Angeles California
United States Local Institution Marietta Georgia
United States Local Institution Miami Florida
United States Local Institution New Brunswick New Jersey
United States Local Institution Redondo Beach California
United States Local Institution Saint Louis Missouri
United States Local Institution Santa Barbara California
United States Local Institution Sioux Falls South Dakota
United States Local Institution Tampa Florida
United States Local Institution Vancouver Washington

Sponsors (1)

Lead Sponsor Collaborator
Bristol-Myers Squibb

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Brazil,  Canada,  Chile,  Colombia,  Germany,  Italy,  Mexico,  Portugal,  Puerto Rico,  Romania,  Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall response rate (ORR) Approximately 31 months
Secondary Incidence of adverse events (AEs) Approximately 5 years
Secondary Incidence of serious adverse events (SAEs) Approximately 5 years
Secondary Incidence of AEs leading to discontinuation Approximately 5 years
Secondary Incidence of deaths Approximately 5 years
Secondary Incidence of laboratory abnormalities Approximately 5 years
Secondary ORR Cohort A1 Approximately 5 years
Secondary Duration of response (DOR) Approximately 5 years
Secondary Progression free survival (PFS) Approximately 5 years
Secondary Overall survival (OS) Approximately 5 years
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