RecruitingPhase 1NCT06476808
A Study to Evaluate the Safety, Tolerability, and Efficacy of Escalating Doses of BMS-986463 in Participants With Select Advanced Malignant Tumors.
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-986463(drug)
- Enrollment
- 240 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2028
Study locations (16)
- USC/Norris Comprehensive Cancer Center, Los Angeles, California, United States
- Valkyrie Clinical Trials, Los Angeles, California, United States
- John Theurer Cancer Center at Hackensack University Medical Center, Hackensack, New Jersey, United States
- Local Institution - 0045, Columbus, Ohio, United States
- Local Institution - 0046, Dallas, Texas, United States
- BC Cancer Vancouver, Vancouver, British Columbia, Canada
- Princess Margaret Cancer Centre, Toronto, Ontario, Canada
- Centre Hospitalier de l'Université de Montréal, Montreal, Quebec, Canada
- Jewish General Hospital, Montreal, Quebec, Canada
- Local Institution - 0031, Villejuif, Val-de-Marne, France
- Local Institution - 0036, Borddeaux Cedex, France
- Local Institution - 0035, Lyon, France
- Local Institution - 0032, Rozzano, Milano, Italy
- Local Institution - 0033, Milan, Italy
- Local Institution - 0041, Avda.Pio XII 36,, Spain
- +1 more locations on ClinicalTrials.gov
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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