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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 Sep 3, 2026, 7:24 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 9, 2020
Primary completion
Dec 30, 2021
Completion
Jun 29, 2022
Last update posted
Apr 3, 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 3, 2022 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04413942 live on ClinicalTrials.gov.

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