๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-18

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

๐ŸŸข Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Novartis Pharmaceuticals

๐Ÿฉบ 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

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ 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

๐Ÿ“ž 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.

๐Ÿ’ฐ 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.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—