Clinical trial
A Phase 1, Randomized, Double-blind, Placebo-controlled, First-in-human, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Prodrug BMS-986465 and Its Active Derivative, BMS-986464, in Healthy Participants Including Healthy Participants of Japanese Ethnicity and an Open-label Assessment of Food, Formulation, and pH Effects on the Relative Bioavailability of BMS-986465 and BMS-986464
NCT06144697 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 1, Randomized, Double-blind, Placebo-controlled, First-in-human, Single and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Prodrug BMS-986465 and Its Active Derivative, BMS-986464, in Healthy Participants Including Healthy Participants of Japanese Ethnicity and an Open-label Assessment of Food, Formulation, and pH Effects on the Relative Bioavailability of BMS-986465 and BMS-986464
- Lead sponsor
- Bristol-Myers Squibb
- Phase
- Phase 1
- Overall status
- Terminated
- Start date
- January 29, 2024
- Completion date
- October 16, 2024
- Enrollment
- 267 (actual)
- Sites
- 2
Conditions
As the registry lists them; a condition with its own page is linked.
healthy participants