๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-29

A Phase 1 Study of Orca-Q in Recipients Undergoing Allogeneic Transplantation for Hematologic Malignancies (NCT03802695)

A Phase 1 Dose Escalation and Expansion Study of Orca-Q, an Engineered Donor Graft Derived From Mobilized Peripheral Blood, in Recipients Undergoing Allogeneic Hematopoietic Cell Transplantation for Hematologic Malignancies

๐ŸŸข Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Orca Biosystems, Inc.

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

This study will evaluate the safety, tolerability, and efficacy of engineered donor grafts ("OrcaGraft"/"Orca-Q") in participants undergoing allogeneic hematopoietic cell transplant (alloHCT) transplantation for hematologic malignancies.

Who can join: Review the eligibility criteria below.

Location: City of Hope โ€” Duarte, California

Age range: 12 Years to 78 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 (12 Sites)

  • City of Hope โ€” Duarte, California
  • UC Davis โ€” Sacramento, California
  • Stanford Health Care โ€” Stanford, California
  • Moffitt Cancer Center โ€” Tampa, Florida
  • Emory University โ€” Atlanta, Georgia
  • The University of Kansas Hospital โ€” Kansas City, Kansas
  • John Theurer Cancer Center at Hackensack University Medical Center โ€” Hackensack, New Jersey
  • Memorial Sloan Kettering Cancer Center โ€” New York, New York
  • Ohio State University โ€” Columbus, Ohio
  • University of Texas MD Anderson Cancer Center โ€” Houston, Texas
  • Fred Hutchinson Cancer Center โ€” Seattle, Washington
  • Froedtert Memorial Lutheran Hospital โ€” Milwaukee, Wisconsin

๐Ÿ“ž Contact the Study Coordinator

Phone: (650) 246-9601

Email: info@orcabiosystems.com

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†—