๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-20

A Study to Evaluate the Safety and Efficacy of Axatilimab in Combination With Ruxolitinib in Participants With Newly Diagnosed Chronic Graft-Versus-Host Disease (NCT06388564)

A Phase 2, Open-Label, Randomized, Multicenter Study to Evaluate the Safety and Efficacy of Axatilimab in Combination With Ruxolitinib in Participants With Newly Diagnosed Chronic Graft-Versus-Host Disease

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Incyte Corporation

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This study will be conducted to determine the preliminary efficacy of axatilimab in combination with ruxolitinib and to assess the contribution of axatilimab to the combination treatment effect in participants with cGVHD.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic Hospital โ€” Phoenix, Arizona

Age range: 12 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 (68 Sites)

Showing the first 25 of 68 sites.

  • Mayo Clinic Hospital โ€” Phoenix, Arizona
  • City of Hope Medical Center โ€” Duarte, California
  • University of California-Los Angeles Medl Cntr-Oncology Center Bowyer Clinic โ€” Los Angeles, California
  • Stanford Cancer Center โ€” Stanford, California
  • University of Colorado Cancer Center โ€” Aurora, Colorado
  • Colorado Blood Cancer Institute โ€” Denver, Colorado
  • Smilow Cancer Center-Yale โ€” New Haven, Connecticut
  • Mayo Clinic Jacksonville โ€” Jacksonville, Florida
  • Northwestern University โ€” Chicago, Illinois
  • The University of Chicago Medicine โ€” Chicago, Illinois
  • University of Maryland-Greenebaum Cancer Center โ€” Baltimore, Maryland
  • Washington University โ€” St Louis, Missouri
  • Fred and Pamela Buffett Cancer Center โ€” Omaha, Nebraska
  • Memorial Sloan Kettering Cancer Center โ€” New York, New York
  • Weill Cornell Medicine โ€” New York, New York
  • Mount Sinai Hospital โ€” New York, New York
  • Cleveland Clinic โ€” Cleveland, Ohio
  • The Ohio State University โ€” Columbus, Ohio
  • University of Pennsylvania Abramson Cancer Center โ€” Philadelphia, Pennsylvania
  • Hillman Cancer Center โ€” Pittsburgh, Pennsylvania
  • Vanderbilt University Medical Center โ€” Nashville, Tennessee
  • Md Anderson Cancer Center โ€” Houston, Texas
  • Fred Hutchinson Cancer Center โ€” Seattle, Washington
  • University of Washington โ€” Seattle, Washington
  • Froedtert & the Medical College of Wisconsin โ€” Milwaukee, Wisconsin

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

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†—