drugset / Trial / NCT04684654

BMS-986325 in Healthy Participants and Participants With Primary Sjögren's Syndrome

NCT04684654 ↗

Phase 1 Terminated 118 enrolled Bristol-Myers Squibb
RandomizedSequentialQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, drug levels, and drug effects of BMS-986325 in healthy participants and participants with primary Sjögren's syndrome. The results will guide the future clinical development with BMS-986325.

Timeline

Start
2021-02-16
Primary completion
2023-07-25
Completion
2023-07-25

Outcome

Outcome not reported

Stopped (Enrollment): “Insufficient enrollment”

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-986325 Unknown — Subcutaneous

Indications