drugset / Trial / NCT04504448

A Study of HNC664 in Healthy Subjects to Evaluate the Safety, Tolerability, and Pharmacokinetics

NCT04504448 ↗

Phase 1 Completed 45 enrolled Guangzhou Henovcom Bioscience Co. Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this First-in-Human study is to evaluate the safety , tolerability,PK and PD after single ascending of HNC664 given to healthy subjects, compared to placebo. Also, food effect will be evaluated.

Timeline

Start
2020-08-11
Primary completion
2021-07-13
Completion
2021-07-13

Drugs

EvaluationDrugModalityDoseRoute
Subject HNC664 Unknown 40 mg Oral
Subject HNC664 Unknown 500 mg Oral

Indications

No indication recorded.