drugset / Trial / NCT03142165

A Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of BMS-986263 in Healthy Participants

NCT03142165

Phase 1 Completed 33 enrolled Bristol-Myers Squibb
RandomizedParallel-groupQuadruple-blindScreening

Summary

The purpose of this study is to assess the safety and tolerability of BMS-986263 in healthy volunteers.

Timeline

Start
2017-05-11
Primary completion
2017-11-29
Completion
2017-11-29

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986263 Small interfering RNA (siRNA) 90 mg Intravenous
Background Diphenhydramine Unknown 50 mg Intravenous
Background Famotidine Other / unclassified 20 mg Intravenous

Indications

No indication recorded.