drugset / Trial / NCT04312568

Evaluate Safety, Tolerability and Pharmacokinetics of Fadanafil (XZP-5849)in Chinese Healthy Adult Male Subjects

NCT04312568 ↗

Phase 1 Completed 66 enrolled Sihuan Pharmaceutical Holdings Group Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety , tolerability, and pharmacokinetics of ascending single dose Fadanafil (XZP-5849)in Chinese healthy adult male subjects. This is the first XZP-5849 clinical study

Timeline

Start
2018-08-10
Primary completion
2018-12-07
Completion
2018-12-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Fadanafil Unknown 12.5 mg —
Subject Fadanafil Unknown 25 mg —
Subject Fadanafil Unknown 50 mg —
Subject Fadanafil Unknown 100 mg —
Subject Fadanafil Unknown 200 mg —
Subject Fadanafil Unknown 300 mg —
Subject Fadanafil Unknown 400 mg —
Subject Fadanafil Unknown 500 mg —

Indications

No indication recorded.