drugset / Trial / NCT07175506

Study of CM559 in Healthy Subjects

NCT07175506 ↗

Phase 1 Recruiting 40 enrolled Keymed Biosciences Co.Ltd
RandomizedSequentialQuadruple-blindTreatment

Summary

This study is a single center, randomized, double-blind, placebo-controlled, single dose, dose escalation Phase I clinical study aimed at evaluating the safety, tolerability, pharmacokinetics, pharmacodynamics, and immunogenicity of CM559 administered intravenously at different doses in healthy male subjects.

Timeline

Start
2025-09
Primary completion
2026-06
Completion
2026-06

Drugs

EvaluationDrugModalityDoseRoute
Subject CM559 Unknown — Intravenous

Indications

No indication recorded.