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Not listed Phase 2 Interventional

Evaluate Efficacy, PK, and Safety of FB825 in Adults With Atopic Dermatitis

ClinicalTrials.gov ID: NCT04413942

Public ClinicalTrials.gov record NCT04413942. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 10:28 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-Blind, Placebo-Controlled Phase II Study to Evaluate Efficacy, Pharmacokinetics, and Safety of Multiple Intravenous Doses of FB825 in Adults With Atopic Dermatitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The study aims to evaluate the efficacy, improvement from baseline in Eczema Area and Severity Index (EASI) score, of multiple intravenous (IV) doses of FB825 in subjects with atopic dermatitis

Study identification

NCT ID
NCT04413942
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Oneness Biotech Co., Ltd.
Industry
Enrollment
99 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 10, 2020 (Actual)
Primary completion
Dec 31, 2021 (Actual)
Completion
Jun 30, 2022 (Estimated)
Last update posted
Apr 4, 2022

2020 – 2022

United States locations

U.S. sites
18
U.S. states
5
U.S. cities
16
Facility City State ZIP Site status
Zenith Research Beverly Hills California 90212 —
Encino Research Center Encino California 91436 —
Marvel Research 002, LLC Huntington Beach California 92647 —
Providence Clinical Research North Hollywood California 91606 —
ACRC Studies San Diego California 92119 —
Unison Clinical Trials Sherman Oaks California 991403 —
University Clinical Research - Deland, LLC DeLand Florida 32720 —
FXM Clinical Research Ft. Lauderdale, LLC. Fort Lauderdale Florida 33308 —
Sweet Hope Research Specialty Hialeah Florida 33016 —
Universal Axon - Homestead, LLC Homestead Florida 33030 —
FXM Clinical Research Miramar, LLC Miramar Florida 33027 —
FXM Clinical Research Miami, LLC Miramar Florida 33175 —
Moore Clinical Research Tampa Florida 33609 —
Avita Clinical Research (PCRS Network) Tampa Florida 33613 —
Oakland Hills Dermatology (PCRS Network) Auburn Hills Michigan 48326 —
Revival Research Institute, LLC Troy Michigan 48084 —
Paddington Testing Co, Inc Philadelphia Pennsylvania 19103 —
Clinical Research Partners Richmond Virginia 23226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04413942, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 4, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04413942 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →