drugset / Trial / NCT03055403

First-in-Human Dose Escalation Study of M201-A in Healthy Japanese Subjects

NCT03055403 ↗

Phase 1 Completed 40 enrolled Yuji KUMAGAI Aetas Pharma Co. Ltd. · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase I first-in-human is designed to evaluate the safety, tolerability and pharmacokinetics of single ascending doses of M201-A administered by single continuous intravenous injection in Healthy Japanese subjects.

Timeline

Start
2017-02-17
Primary completion
2017-11-28
Completion
2017-11-28

Drugs

EvaluationDrugModalityDoseRoute
Subject M201-A Unknown — Intravenous

Indications

No indication recorded.