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RECRUITING
NCT07325136
PHASE1/PHASE2

A Study to Assess the Safety and Tolerability of BMS-986525 Alone and in Combination With Nivolumab in Participants With Relapsed/Refractory Small Cell Lung Cancer

Sponsor: Bristol-Myers Squibb

View on ClinicalTrials.gov

Summary

The purpose of this study is to assess the safety and tolerability of BMS-986525 alone and in combination with Nivolumab in participants with Relapsed/Refractory Small Cell Lung Cancer

Official title: A Phase 1/2 Study of BMS-986525 as Monotherapy and in Combination With Nivolumab in Participants With Relapsed/Refractory Small Cell Lung Cancer

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

240

Start Date

2026-02-03

Completion Date

2029-04-24

Last Updated

2026-03-09

Healthy Volunteers

No

Interventions

DRUG

BMS-986525

Specified dose on specified days

DRUG

Nivolumab

Specified dose on specified days

Locations (11)

Local Institution - 0011

Detroit, Michigan, United States

Local Institution - 0026

Buffalo, New York, United States

Local Institution - 0005

Durham, North Carolina, United States

University Hospitals Cleveland Medical Center

Cleveland, Ohio, United States

SCRI Oncology Partners

Nashville, Tennessee, United States

Local Institution - 0001

Rozzano, Milano, Italy

Local Institution - 0020

Hirakata, Osaka, Japan

Local Institution - 0018

Chuo-ku, Tokyo, Japan

Local Institution - 0023

Timișoara, Timiș County, Romania

Local Institution - 0003

Craiova, Romania

Local Institution - 0009

Madrid, Spain