drugset / Trial / NCT05088369

Assessment of the Safety, Tolerability, and Pharmacokinetic of HM201

NCT05088369 ↗

Phase 1 Completed 53 enrolled Syneos Health Himuka AM Pharma Corp. · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This will be a single centre, Phase 1, Placebo-controlled, Randomized, Doubleblind, SAD \& MAD Study to Assess the Safety, Tolerability and PK of HM201 in Healthy Subjects.

Timeline

Start
2021-11-11
Primary completion
2022-12-19
Completion
2022-12-19

Drugs

EvaluationDrugModalityDoseRoute
Subject HM201 Unknown 0.01 mg/kg Intravenous
Subject HM201 Unknown 0.03 mg/kg Intravenous
Subject HM201 Unknown 0.06 mg/kg Intravenous
Subject HM201 Unknown 0.12 mg/kg Intravenous