Overview

Study in Subjects to Evaluate the Safety, Tolerability and Pharmacokinetics of GT20029

Status:
Recruiting
Trial end date:
2023-02-10
Target enrollment:
Participant gender:
Summary
A randomized, double-blind, Placebo-controlled, parallel group, dose escalation study to evaluate the safety, tolerability and pharmacokinetics (PK) of GT20029 following topical single ascending dose in healthy subjects and multiple ascending dose administration in subjects with androgenetic alopecia(AGA) or acne
Phase:
Phase 1
Details
Lead Sponsor:
Suzhou Kintor Pharmaceutical Inc,