drugset / Trial / NCT03740555

A Study of HNC042 in Healthy Subjects to Evaluate the Safety, Tolerability, and Pharmacokinetics.

NCT03740555 ↗

Phase 1 Completed 74 enrolled Guangzhou Henovcom Bioscience Co. Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this First-in-Human study is to evaluate the safety , tolerability and pharmacokinetics after single ascending of HNC042 given to healthy subjects, compared to placebo. Also, the safety , tolerability and pharmacokinetics of multiple ascending of HNC042 given to healthy subjects daily for 7 days compared to placebo , will be evaluated.

Timeline

Start
2018-11-09
Primary completion
2019-07-19
Completion
2019-07-19

Drugs

EvaluationDrugModalityDoseRoute
Subject HNC042 Unknown 100 mg Intravenous
Subject HNC042 Unknown 300 mg Intravenous
Subject HNC042 Unknown 1200 mg Intravenous

Indications

No indication recorded.