drugset / Trial / NCT05638282

A Study to Evaluate the Safety and Tolerability of Cendakimab in Chinese Healthy Participants

NCT05638282 ↗

Phase 1 Completed 25 enrolled Bristol-Myers Squibb
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the drug levels, safety, and tolerability of cendakimab in healthy male and female Chinese participants.

Timeline

Start
2023-02-15
Primary completion
2023-06-27
Completion
2023-06-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Cendakimab Monoclonal antibody — Subcutaneous

Indications

No indication recorded.