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Completed Phase 2 Interventional

Phase 2b Safety and Efficacy Study of CGB-500 Topical Ointment With 0.5% and 1% Tofacitnib for Treatment of Atopic Dermatitis

ClinicalTrials.gov ID: NCT06810050

Public ClinicalTrials.gov record NCT06810050. 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, 3:23 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

Safety and Effectiveness of CGB-500 Topical Ointment With 0.5% and 1% Tofacitinib for the Treatment of Atopic Dermatitis: A Randomized, Dose-Ranging, Vehicle-Controlled, Double-Blind Trial

Brief summary

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

The goal of this clinical trial is to learn if CGB-500 works to treat atopic dermatitis in participants ages 12 and older. The goal is also to learn about the safety of CGB-500. The main questions it aims to answer are: Does CGB-500 improve atopic dermatitis by decreasing the area affected and the severity of the lesions? What medical problems do participants have when taking CGB500? Researchers will compare CGB-500 to a placebo (a look-alike substance that contains no drug) to see if CGB-500 works to treat atopic dermatitis. Participants will: Take CGB-500 or a placebo every day for 8 weeks. Visit the clinic once every 2 weeks for the first month and at the end of 8 weeks. Keep a diary of when they use the product and complete a form about their symptoms including itching.

Study identification

NCT ID
NCT06810050
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
CAGE Bio Inc.
Industry
Enrollment
180 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
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
Dec 17, 2024
Primary completion
Aug 29, 2025
Completion
Oct 29, 2025
Last update posted
Apr 1, 2026

2024 – 2025

United States locations

U.S. sites
16
U.S. states
8
U.S. cities
16
Facility City State ZIP Site status
Center for Dermatology Clinical Research Inc. Fremont California 94538
Ablon Skin Institute and Research Center Manhattan Beach California 90266
TCR Medical Corporation San Diego California 92123
Syrentis Clinical Research Santa Ana California 92705
USA and International Research Inc. Doral Florida 33126
FXM Clinical Research Fort Lauderdale Florida 33308
Driven Research Gables Florida 33134
FXM Clinical Research Miami, LLC Miami Florida 33175
FXM Clinical Research Miramar, LLC Miramar Florida 33027
Cordova Research Institute Sweetwater Florida 33182
The Indiana Clinical Trials Center, PC Plainfield Indiana 46168
Metro Boston Clinical Partners Brighton Massachusetts 02135
J&S Studies, Inc. New Brighton Minnesota 55112
JDR Dermatology Research Las Vegas Nevada 89148
Tennessee Clinical Research Center Nashville Tennessee 37215
DermResearch Austin Texas 78759

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 NCT06810050, 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 1, 2026 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06810050 live on ClinicalTrials.gov.

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