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Not listed Phase 2 Interventional

Phase 2a Study of Efficacy and Safety of OpSCF in Moderate to Severe Atopic Dermatitis

ClinicalTrials.gov ID: NCT06101823

Public ClinicalTrials.gov record NCT06101823. 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 1, 2026, 11:04 PM 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 2a Study to Evaluate the Efficacy and Safety of OpSCF in the Treatment of Adult Subjects With Moderate to Severe Atopic Dermatitis

Brief summary

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

The purpose of this study is to determine the efficacy and safety of a monoclonal antibody, OpSCF, in the treatment of adults with moderate to severe Atopic Dermatitis (Eczema). OpSCF will be compared to a placebo. OpSCF or placebo will be administered every 2 weeks for 14 weeks, and the efficacy will be assessed two weeks later. After that, subjects may choose to enter an Open Label Extension phase in which all subjects will receive OpSCF every 4 weeks for 40 additional weeks.

Study identification

NCT ID
NCT06101823
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Opsidio, LLC
Industry
Enrollment
48 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 75 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
Oct 24, 2023
Primary completion
Sep 30, 2024
Completion
May 31, 2025
Last update posted
May 6, 2024

2023 – 2025

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Cahaba Dermatology & Skin Health Center Birmingham Alabama 33607
First OC Dermatology Research Fountain Valley California 92708
Axon Clinical Research Inglewood California 90301
University Clinical Trials San Diego California 92123
Unison Clinical Trials Sherman Oaks California 91403
Skin Care Research Boca Raton Florida 33456
Skin Research of South Florida Miami Florida 33173
RM Medical Research Miami Lakes Florida 33014
Advanced Clinical Research Institute Tampa Florida 33607
Arlington Dermatology Rolling Meadows Illinois 60008
Options Research Group West Lafayette Indiana 47906
DS Research of Kentucky Louisville Kentucky 40241
Oakland Hills Dermatology P.C Auburn Hills Michigan 48326
Saginaw Bay Dermatology Bay City Michigan 48706
Skin Cancer and Dermatology Institute Reno Nevada 89509
Forest Hills Dermatology Group Kew Gardens New York 11415
Rodgers Dermatology Frisco Texas 75034
Dermatology Of Seattle Bellevue Washington 98004

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06101823, 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 May 6, 2024 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06101823 live on ClinicalTrials.gov.

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