Clinical trial
A Phase I/2a Dose Escalation and Cohort Expansion Study of the Safety, Tolerability, and Efficacy of Anti-LAG-3 Monoclonal Antibody (BMS-986016) Administered Alone and in Combination With Anti-PD-1 Monoclonal Antibody (Nivolumab, BMS-936558) in Advanced Solid Tumors
NCT01968109 is registered in ClinicalTrials.gov with Bristol-Myers Squibb as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase I/2a Dose Escalation and Cohort Expansion Study of the Safety, Tolerability, and Efficacy of Anti-LAG-3 Monoclonal Antibody (BMS-986016) Administered Alone and in Combination With Anti-PD-1 Monoclonal Antibody (Nivolumab, BMS-936558) in Advanced Solid Tumors
- Lead sponsor
- Bristol-Myers Squibb
- Phase
- Phase 1/2
- Overall status
- Completed
- Start date
- November 5, 2013
- Completion date
- February 3, 2025
- Enrollment
- 1,482 (actual)
- Sites
- 54
Conditions
As the registry lists them; a condition with its own page is linked.