drugset / Trial / NCT05371379

Multiple Ascending Dose Study of CM338 in Healthy Volunteers

NCT05371379 ↗

Phase 1 Completed 48 enrolled Keymed Biosciences Co.Ltd
RandomizedSequentialQuadruple-blindTreatment

Summary

This study was a multi-center, randomized, double blind, placebo-controlled, single-dose, dose escalation Phase I study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of CM338 with multiple dosing in healthy subjects.

Timeline

Start
2022-05-24
Primary completion
2022-11-04
Completion
2022-11-04

Drugs

EvaluationDrugModalityDoseRoute
Subject CM338 Monoclonal antibody 75 mg Subcutaneous
Subject CM338 Monoclonal antibody 150 mg Subcutaneous
Subject CM338 Monoclonal antibody 300 mg Subcutaneous

Indications

No indication recorded.