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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
2026-05-07
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
Duke Cancer Institute
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