drugset / Trial / NCT06161090

Study of CM310 in Healthy Subjects

NCT06161090

Phase 1 Completed 33 enrolled Keymed Biosciences Co.Ltd
Non-randomizedSequentialQuadruple-blindTreatment

Summary

This is a single center, randomized, double-blind, placebo-controlled, dose escalation study.

Timeline

Start
2019-09-03
Primary completion
2020-01-13
Completion
2020-01-13

Drugs

EvaluationDrugModalityDoseRoute
Subject CM310 Monoclonal antibody 75 mg Subcutaneous
Subject CM310 Monoclonal antibody 150 mg Subcutaneous
Subject CM310 Monoclonal antibody 300 mg Subcutaneous
Subject CM310 Monoclonal antibody 600 mg Subcutaneous

Indications

No indication recorded.