drugset / Trial / NCT04502901

the Safety, Tolerability and PK of KX-826 in Healthy Males With Alopecia Following Topical Multiple Dose Ascending

NCT04502901 ↗

Phase 1 Completed 40 enrolled Suzhou Kintor Pharmaceutical Inc
RandomizedParallel-groupTriple-blindTreatment

Summary

The study is a randomized, double-blind, placebo-controlled, dose-escalation study to evaluate the safety, tolerability and PK of KX-826 following topical multiple ascending dose administration.

Timeline

Start
2020-01-14
Primary completion
2020-08-11
Completion
2021-01-15

Drugs

EvaluationDrugModalityDoseRoute
Subject KX0826 Unknown 2.5 mg Topical
Subject KX0826 Unknown 5 mg Topical
Subject KX0826 Unknown 10 mg Topical
Subject KX0826 Unknown 20 mg Topical

Indications