๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2023-07-18

Study of Iomab-B vs. Conventional Care in Older Subjects With Active, Relapsed or Refractory Acute Myeloid Leukemia (NCT02665065)

A Multicenter, Pivotal Phase 3 Study of Iomab-B Prior to Allogeneic Hematopoietic Cell Transplant Versus Conventional Care in Older Subjects With Active, Relapsed or Refractory Acute Myeloid Leukemia (AML)

๐Ÿ”ต Active, Not Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Actinium Pharmaceuticals

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

The primary objective of this study is to demonstrate the efficacy of Iomab-B, in conjunction with a Reduced Intensity Conditioning (RIC) regimen and protocol-specified allogeneic hematopoietic stem cell transplant (HCT), versus Conventional Care in patients with Active, Relapsed or Refractory Acute Myeloid Leukemia (AML).

Who can join: Review the eligibility criteria below.

Location: Banner MD Anderson Cancer Center โ€” Gilbert, Arizona

Age range: 55 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 (24 Sites)

  • Banner MD Anderson Cancer Center โ€” Gilbert, Arizona
  • Yale Cancer Center โ€” New Haven, Connecticut
  • Georgetown University Medical Center โ€” Washington D.C., District of Columbia
  • Mayo Clinic โ€” Jacksonville, Florida
  • Loyola University Medical Center โ€” Maywood, Illinois
  • University of Iowa โ€” Iowa City, Iowa
  • The University of Kansas Cancer Center โ€” Westwood, Kansas
  • Mayo Clinic โ€” Rochester, Minnesota
  • Washington University School of Medicine โ€” St Louis, Missouri
  • University of Nebraska Medical Center โ€” Omaha, Nebraska
  • Roswell Park Cancer Institute โ€” Buffalo, New York
  • Weill Cornell Medicine โ€” New York, New York
  • Memorial Sloan Kettering Cancer Center โ€” New York, New York
  • Stony Brook University โ€” Stony Brook, New York
  • University of North Carolina Hospital โ€” Chapel Hill, North Carolina
  • University Hospital of Cleveland Seidman Cancer Center โ€” Cleveland, Ohio
  • The Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio
  • Oregon Health & Science University โ€” Portland, Oregon
  • Baylor Charles A. Sammons Cancer Center โ€” Dallas, Texas
  • MD Anderson Cancer Center โ€” Houston, Texas
  • Fred Hutchinson Cancer Research Center โ€” Seattle, Washington
  • Medical College of Wisconsin โ€” Milwaukee, Wisconsin
  • University of Ottawa โ€” Ottawa, Ontario
  • Princess Margaret Cancer Centre โ€” Toronto, Ontario

๐Ÿ“ž Contact the Study Coordinator

Phone: (877) 632-6789

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†—