drugset / Trial / NCT05803850

A Study to Evaluate the Safety, Tolerability, PK and PD of HNC1058

NCT05803850 ↗

Phase 1 Completed 32 enrolled Guangzhou Henovcom Bioscience Co. Ltd.
RandomizedSequentialQuadruple-blindTreatment

Summary

The purpose of this First-in-Human study is to evaluate the safety and tolerability after single ascending oral doses of HNC1058 given to healthy subjects, compared to placebo.

Timeline

Start
2023-03-28
Primary completion
2024-02-27
Completion
2024-03-08

Drugs

EvaluationDrugModalityDoseRoute
Subject HNC1058 Unknown 10 mg Oral
Subject HNC1058 Unknown 50 mg Oral
Subject HNC1058 Unknown 80 mg Oral