Platform Study to Evaluate the Efficacy and Safety of Investigational Compound(s) in Patients With Moderate to Severe Atopic Dermatitis (NCT06947993)
A Multicenter, Randomized, Double-blind, Placebo-controlled, Phase II Platform Study to Assess the Efficacy and Safety of Investigational Compound(s) in Patients With Moderate to Severe Atopic Dermatitis
๐ฉบ Plain-English Summary (8th-Grade Level)
This trial is designed to evaluate multiple compounds in participants with moderate to severe atopic dermatitis (AD).
Who can join: Review the eligibility criteria below.
Location: Novartis Investigative Site โ Birmingham, Alabama
Age range: 18 Years to 100 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (105 Sites)
Showing the first 25 of 105 sites.
- Novartis Investigative Site โ Birmingham, Alabama
- Novartis Investigative Site โ Birmingham, Alabama
- Novartis Investigative Site โ Fort Smith, Arkansas
- Novartis Investigative Site โ Fountain Valley, California
- Novartis Investigative Site โ Los Angeles, California
- Novartis Investigative Site โ Sacramento, California
- Novartis Investigative Site โ Santa Ana, California
- Novartis Investigative Site โ Santa Monica, California
- Novartis Investigative Site โ Washington D.C., District of Columbia
- Novartis Investigative Site โ Miami, Florida
- Novartis Investigative Site โ St. Petersburg, Florida
- Novartis Investigative Site โ Atlanta, Georgia
- Novartis Investigative Site โ Macon, Georgia
- Novartis Investigative Site โ Louisville, Kentucky
- Novartis Investigative Site โ Brighton, Massachusetts
- Novartis Investigative Site โ Troy, Michigan
- Novartis Investigative Site โ Saint Joseph, Missouri
- Novartis Investigative Site โ Portsmouth, New Hampshire
- Novartis Investigative Site โ Brooklyn, New York
- Novartis Investigative Site โ Arlington, Texas
- Novartis Investigative Site โ Cypress, Texas
- Novartis Investigative Site โ Dallas, Texas
- Novartis Investigative Site โ Houston, Texas
- Novartis Investigative Site โ San Antonio, Texas
- Novartis Investigative Site โ Caba, Buenos Aires
๐ Contact the Study Coordinator
Phone: (888) 669-6682
Email: novartis.email@novartis.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Atopic Dermatitis
- A Study to See How Well Lebrikizumab Works in Adults and Adolescents With Moderate Atopic Dermatitis (Eczema) and High Itch Burden โ Birmingham, Alabama
- ATI-045 Versus Placebo in Patients With Moderate-to-Severe Atopic Dermatitis โ Phoenix, Arizona
- A Study of Barzolvolimab in Patients With Atopic Dermatitis โ Birmingham, Alabama
- Defining the Skin and Blood Biomarkers of Pediatric Atopic Dermatitis โ Chicago, Illinois
- A Study of KT-621 Administered Orally to Participants With Moderate to Severe Atopic Dermatitis โ Birmingham, Alabama
- A Study Evaluating APG777 in Atopic Dermatitis โ Fountain Valley, California
Explore by condition: All Atopic Dermatitis clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.