🏛️ Verified NIH Record • Updated 2026-05-07

Cusatuzumab in Combination With Background Therapy for the Treatment of Participants With Acute Myeloid Leukemia (NCT04150887)

An Open-label, Multicenter, Phase 1b Study of OV-1001 (Cusatuzumab; Anti-CD70 Monoclonal Antibody) in Combination With Background Therapy for the Treatment of Subjects With Acute Myeloid Leukemia

🔵 Active, Not Recruiting Phase1 💊 Investigational Drug / Biologic Sponsor: OncoVerity, Inc.

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

The purpose of the study is to characterize safety and tolerability of cusatuzumab in combination with various therapies used to treat acute myeloid leukemia (AML).

Who can join: Review the eligibility criteria below.

Location: City of Hope — Duarte, California

Age range: 18 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 (23 Sites)

  • City of Hope — Duarte, California
  • Norton Cancer Institute — Louisville, Kentucky
  • Barbara Ann Karmanos Cancer Institute — Detroit, Michigan
  • Roswell Park Cancer Institute — Buffalo, New York
  • Weill Cornell Medicine — New York, New York
  • Memorial Sloan Kettering Cancer Center — New York, New York
  • University of Rochester — Rochester, New York
  • University of Pittsburgh School of Medicine — Pittsburgh, Pennsylvania
  • The University of Texas MD Anderson Cancer Center — Houston, Texas
  • University of Vermont — Burlington, Vermont
  • Wisconsin Medical Center — Milwaukee, Wisconsin
  • Tom Baker Cancer Centre — Calgary, Alberta
  • University of Alberta Hospital — Edmonton, Alberta
  • University of Toronto — Toronto, Ontario
  • McGill University Health Centre — Montreal, Quebec
  • Universitaetsklinik Hamburg-Eppendorf — Hamburg,
  • Universitaetsklinikum Leipzig — Leipzig,
  • Klinikum der Universitaet Muenchen — München,
  • Szpital Uniwersytecki w Krakowie — Krakow,
  • Wojewodzkie Wielospecjalistyczne Centrum Onkologii i Traumatologii im. M. Kopernika w Lodzi — Lodz,
  • Instytut Hematologii i Transfuzjologii — Warsaw,
  • INSELSPITAL, Universitätsspital Bern — Bern,
  • Kantonsspital St.Gallen — Sankt Gallen,

📞 Contact the Study Coordinator

Phone: (800) 826-4673

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 ↗