drugset / Trial / NCT06117514

Sudapyridine (WX-081) in Healthy Volunteers

NCT06117514 ↗

Phase 1 Completed 82 enrolled Shanghai Jiatan Pharmatech Co., Ltd
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of this study is to evaluate the safety, tolerability as well as pharmacokinetics of Sudapyridine (WX-081) in Chinese volunteers.

Timeline

Start
2019-02-13
Primary completion
2020-07-02
Completion
2020-07-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Sudapyridine Unknown 30 mg Oral
Subject Sudapyridine Unknown 100 mg Oral
Subject Sudapyridine Unknown 200 mg Oral
Subject Sudapyridine Unknown 300 mg Oral

Indications

No indication recorded.