๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-03-24

Ruxolitinib + Allogeneic Stem Cell Transplantation in AML (NCT03286530)

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Massachusetts General Hospital

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

This research study is studying a drug that may help decrease the chances of relapse after Allogeneic Stem Cell transplantation for Acute Myeloid Leukemia. The name of the study drug involved in this study is: โ€ข Ruxolitinib

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (21 items) and avoid the listed exclusions (17 items).

Location: Beth Israel Deaconess Medical Center โ€” Boston, Massachusetts

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

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Usually NOT eligible if any of the following apply:

  • Exclusion Criteria:
  • Have had a prior allogeneic HSCT.
  • Patients without normal organ function defined as follows:
  • AST (SGOT), ALT (SGPT) and Alkaline Phosphatase \>3 ร— institutional Upper Limit of Normal (ULN)
  • Direct bilirubin \>2.0 mg/dL
  • Adequate renal function as defined by calculated creatinine clearance โ‰ค 40 mL/min (Cockcroft-Gault formula)
  • Have a history of other malignancy(ies) unless:
  • They have been disease-free for at least 5 years and are deemed by the treating investigator to be at low risk for recurrence of that malignancy, \--- or
  • The only cancer they have had is cervical cancer in situ, or basal cell or squamous cell carcinoma of the skin
  • Have a chronic or active infection that requires systemic antibiotics, antifungal or antiviral treatment.
  • Have current or a history of congestive heart failure New York Heart Association (NYHA) class 3 or 4, or any history of documented diastolic or systolic dysfunction (LVEF \< 40%, as measured by MUGA scan or echocardiogram)
  • Have an uncontrolled intercurrent illness including, but not limited to, ongoing infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.

๐Ÿ” Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

๐Ÿ“ All Participating Trial Locations (6 Sites)

  • Beth Israel Deaconess Medical Center โ€” Boston, Massachusetts
  • Massachusetts General Hospital โ€” Boston, Massachusetts
  • Washington University โ€” St Louis, Missouri
  • The Ohio State University โ€” Columbus, Ohio
  • Vanderbilt University โ€” Nashville, Tennessee
  • Medical College of Wisconsin โ€” Wauwatosa, Wisconsin

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›๏ธ View Official NIH Record โ†—