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NOT YET RECRUITING
NCT07449156
PHASE1/PHASE2

A Study to Evaluate Efficacy and Safety of HB0043 in Aadult Patients With Moderate to Severe Acne Vulgaris.

Sponsor: Shanghai Huaota Biopharmaceutical Co., Ltd.

View on ClinicalTrials.gov

Summary

The purpose of this study is to assess efficacy safety and tolerability of HB0043 in adult patients with moderate to severe AV.

Official title: A Phase I, Single-center, Randomized, Double-blind, Placebo-controlled Clinical Trial to Evaluate the Safety and Efficacy of HB0043 (Bispecific Antibody Targeting IL-17A and IL-36R) in Adult Patients With Moderate to Severe Acne Vulgaris (AV).

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

21

Start Date

2026-03-27

Completion Date

2027-03-27

Last Updated

2026-03-04

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

HB0043

300mg

DRUG

Placebo

300mg

Locations (1)

Dermatology Hospital affiliated to Shandong First Medical University,

Jinan, Shandong, China