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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
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
BMS-986525
Specified dose on specified days
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