drugset / Trial / NCT07292688

Study of CM383 in Healthy Subjects

NCT07292688 ↗

Phase 1 Recruiting 30 enrolled Keymed Biosciences Co.Ltd
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a Phase I, single-center, randomized, open-label, parallel-controlled study, aimed at evaluating the pharmacokinetics, pharmacodynamics, immunogenicity, safety, and tolerability of a single dose of CM383 administered via intravenous infusion or subcutaneous injection in healthy male subjects.

Timeline

Start
2026-01
Primary completion
2026-07
Completion
2026-07

Drugs

EvaluationDrugModalityDoseRoute
Subject CM383 Unknown — Subcutaneous

Indications

No indication recorded.