🏛️ Verified NIH Record • Updated 2026-08-13

A Study of Enpatoran in Participants With Cutaneous Manifestations of Lupus With or Without Systemic Disease (NCT07332481)

A Phase 3, Randomized, Double-Blind,Placebo-Controlled Parallel Study to Evaluate the Efficacy and Safety of Enpatoran in Participants With Active Cutaneous Manifestations of Lupus Erythematosus With or Without Systemic Disease Receiving Standard of Care (ELOWEN-1)

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: EMD Serono Research & Development Institute, Inc.

🩺 Plain-English Summary (8th-Grade Level)

The purpose of this global, multicenter, Phase 3 study is to evaluate the efficacy and safety of enpatoran over 24 weeks in participants with active cutaneous manifestations of lupus erythematosus with or without systemic disease. Study details include: Study Duration: Up to 35 weeks. Treatment Duration: 24 weeks. Visit Frequency: every 4 weeks, with the exception of the Week 2 televisit. Study Intervention Name: Enpatoran, Placebo. Intervention Form: Film-coated tablet.

Who can join: Review the eligibility criteria below.

Location: Dermatology Research Associates - 300204025 — Los Angeles, California

Age range: 18 Years to 75 Years

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (18 Sites)

  • Dermatology Research Associates - 300204025 — Los Angeles, California
  • Cohen Medical Centers — Thousand Oaks, California
  • GNP Research at Mark Jaffe, MD — Cooper City, Florida
  • Advance Medical Research Center — Miami, Florida
  • Diverse Clinical Research LLC — Miami, Florida
  • D&H National Research Centers, Inc. — Tamarac, Florida
  • Clinical Research of West Florida, Inc. — Tampa, Florida
  • Emory University School of Medicine — Atlanta, Georgia
  • Revival Research Institute, LLC — Troy, Michigan
  • Allen Arthritis — Allen, Texas
  • Arthritis and Rheumatology Research Institute PLLC — Allen, Texas
  • Arthritis Care of Texas — Corpus Christi, Texas
  • JCHO Chukyo Hospital - Dept of Dermatology — Nagoya, Aichi-ken
  • NHO Chibahigashi National Hospital - Dept of Allergy/Rheumatology — Chiba, Chiba
  • Sapporo City General Hospital - Dept of Rheumatology/Immunology — Sapporo, Hokkaido
  • Kanazawa University Hospital - Dept of Rheumatology/Immunology — Kanazawa, Ishikawa-ken
  • St. Luke's International Hospital - Dept of Immunology/Allergy — Chūōku, Tokyo-To
  • Kantonsspital St. Gallen - Klinik f. Dermatologie, Venerologie u Allergologie — Sankt Gallen,

📞 Contact the Study Coordinator

Phone: +49 6151 72 5200

Email: service@emdgroup.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 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 § 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.

💡 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.
🏛️ View Official NIH Record ↗