Evaluate Efficacy and Safety of Repeat Subcutaneous Doses of FB825 in Adults With Moderate-to-Severe Atopic Dermatitis

PHASE2RecruitingINTERVENTIONAL
Enrollment

90

Participants

Timeline

Start Date

August 8, 2024

Primary Completion Date

June 30, 2026

Study Completion Date

June 30, 2026

Conditions
Atopic Dermatitis
Interventions
DRUG

FB825

The study treatment will be administered as 5 SC doses in total 12 weeks

DRUG

Placebo

The study treatment will be administered as 5 SC doses in total 12 weeks

Trial Locations (16)

77401

RECRUITING

UT Health Science Houston, Bellaire

77598

RECRUITING

Center for Clinical Studies, Webster

90025

RECRUITING

California Allergy and Asthma Medical Group, Los Angeles

92708

RECRUITING

First OC Dermatology, Fountain Valley

94538

RECRUITING

Center for Dermatology Clinical Research, Inc., Fremont

95816

RECRUITING

University of California, Davis Health, Department of Dermatology, Sacramento

Unknown

RECRUITING

Kaohsiung Chang Gung Memorial Hospital, Kaohsiung City

RECRUITING

Kaohsiung Veterans General Hospital, Kaohsiung City

RECRUITING

Linkou Chang Gung Memorial Hospital, New Taipei City

RECRUITING

Taipei Medical University-Shuang Ho Hospital, New Taipei City

RECRUITING

China Medical University Hospital, Taichung

RECRUITING

National Cheng Kung University Hospital, Tainan City

RECRUITING

National Taiwan University Hospital, Taipei

RECRUITING

Taipei Mackay Memorial Hospital, Taipei

RECRUITING

Taipei Veterans General Hospital, Taipei

RECRUITING

Tri-Service General Hospital, Taipei

Sponsors
All Listed Sponsors
lead

Oneness Biotech Co., Ltd.

INDUSTRY