To Evaluate the Safety, Tolerability and PK of GT20029 Gel and Solution in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

92

Participants

Timeline

Start Date

July 25, 2021

Primary Completion Date

August 15, 2022

Study Completion Date

April 26, 2023

Conditions
AcneAlopecia
Interventions
DRUG

GT20029

Stage 1: GT20029 gel single ascending dose (1mg, 2mg, 5mg, 10mg) with 14 days washout window; Multi ascending dose (2mg QD, 2mg Q12h, 5mg QD, 5mg Q12h,10mg QD) for 14 consecutive days; Stage 2: GT20029 solution multi ascending dose (5mg QD, 10mg QD, 20mg QD) for 14 consecutive days;

DRUG

GT20029 matching placebo

Stage 1: GT20029 gel matching placebo single ascending dose (1mg, 2mg, 5mg, 10mg) with 14 days washout window; Multi ascending dose (2mg QD, 2mg Q12h, 5mg QD, 5mg Q12h,10mg QD) for 14 consecutive days; Stage 2: GT20029 solution matching placebo multi ascending dose (5mg QD, 10mg QD, 20mg QD) for 14 consecutive days;

Trial Locations (1)

200040

Clinical Pharmacology Research Center, Huashan Hospital, Fudan University, Shanghai

All Listed Sponsors
lead

Suzhou Kintor Pharmaceutical Inc,

INDUSTRY

NCT06468579 - To Evaluate the Safety, Tolerability and PK of GT20029 Gel and Solution in Healthy Subjects | Biotech Hunter | Biotech Hunter