drugset / Trial / NCT02932969

Study With Healthy Japanese and Non-Asian Participants With BMS-986231

NCT02932969

Phase 1 Completed 56 enrolled Bristol-Myers Squibb
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this Phase 1 study is to evaluate the safety, tolerability, PK, and pharmacodynamics (PD) of BMS-986231 in healthy Japanese and Non-Asian participants. There is no formal hypothesis to be statistically tested.

Timeline

Start
2016-10-04
Primary completion
2017-05-26
Completion
2017-05-26

Drugs

EvaluationDrugModalityDoseRoute
Subject cimlanod Other / unclassified Intravenous

Indications