drugset / Trial / NCT05428449

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

NCT05428449 ↗

Phase 1 Completed 123 enrolled Suzhou Kintor Pharmaceutical Inc
RandomizedParallel-groupQuadruple-blindTreatment

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

Timeline

Start
2022-02-10
Primary completion
2022-10-27
Completion
2023-04-06

Drugs

EvaluationDrugModalityDoseRoute
Subject GT20029 Unknown — Topical