RecruitingPHASE1, PHASE2NCT07223047
A Study to Evaluate the Safety, Tolerability, and Efficacy of BMS-986523 Alone and in Combination With Anti-Cancer Agents in Participants With Advanced Solid Malignancies
Studying Small cell lung cancer
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Bristol-Myers Squibb
- Principal Investigator
- Bristol-Myers SquibbBristol-Myers Squibb
- Intervention
- BMS-986523(drug)
- Enrollment
- 252 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2028
Study locations (8)
- Local Institution - 0009, Baltimore, Maryland, United States
- NEXT Oncology, San Antonio, Texas, United States
- START Mountain Region, West Valley City, Utah, United States
- NEXT Virginia, Fairfax, Virginia, United States
- Local Institution - 0002, Vancouver, British Columbia, Canada
- Local Institution - 0010, Toronto, Ontario, Canada
- Local Institution - 0006, Badalona, Barcelona [Barcelona], Spain
- Local Institution - 0008, Hortaleza, Madrid, Spain
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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