drugset / Trial / NCT05337345

A Study to Evaluate the Drug Levels of Cendakimab Delivered Subcutaneously in Healthy Participants

NCT05337345 ↗

Phase 1 Completed 104 enrolled Bristol-Myers Squibb
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the drug levels of cendakimab delivered subcutaneously in healthy participants.

Timeline

Start
2022-05-02
Primary completion
2022-12-15
Completion
2022-12-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Cendakimab Monoclonal antibody 360 mg Subcutaneous

Indications

No indication recorded.