๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-12

Venetoclax for the Treatment of Patients With Relapsed Hairy Cell Leukemia (NCT06311227)

A Phase 2 Study of Venetoclax in Relapsed Classic or Variant Hairy Cell Leukemia

๐ŸŸข Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

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

This phase II trial tests how well venetoclax works in treating patients with hairy cell leukemia that has come back after a period of improvement (relapsed). Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein needed for cancer cell survival.

Who can join: Review the eligibility criteria below.

Location: City of Hope Comprehensive Cancer Center โ€” Duarte, California

Age range: 18 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 (21 Sites)

  • City of Hope Comprehensive Cancer Center โ€” Duarte, California
  • City of Hope at Irvine Lennar โ€” Irvine, California
  • UM Sylvester Comprehensive Cancer Center at Aventura โ€” Aventura, Florida
  • UM Sylvester Comprehensive Cancer Center at Coral Gables โ€” Coral Gables, Florida
  • UM Sylvester Comprehensive Cancer Center at Coral Springs โ€” Coral Springs, Florida
  • UM Sylvester Comprehensive Cancer Center at Deerfield Beach โ€” Deerfield Beach, Florida
  • UM Sylvester Comprehensive Cancer Center at Doral โ€” Doral, Florida
  • UM Sylvester Comprehensive Cancer Center at Hollywood โ€” Hollywood, Florida
  • University of Miami Miller School of Medicine-Sylvester Cancer Center โ€” Miami, Florida
  • UM Sylvester Comprehensive Cancer Center at Kendall โ€” Miami, Florida
  • University of Kansas Cancer Center โ€” Kansas City, Kansas
  • University of Kansas Cancer Center-Overland Park โ€” Overland Park, Kansas
  • University of Kansas Hospital-Westwood Cancer Center โ€” Westwood, Kansas
  • University of Maryland/Greenebaum Cancer Center โ€” Baltimore, Maryland
  • NCI - Center for Cancer Research โ€” Bethesda, Maryland
  • University of Kansas Cancer Center - Briarcliff โ€” Kansas City, Missouri
  • University of Kansas Cancer Center - North โ€” Kansas City, Missouri
  • University of Kansas Cancer Center - Lee's Summit โ€” Lee's Summit, Missouri
  • University of Cincinnati Cancer Center-UC Medical Center โ€” Cincinnati, Ohio
  • Ohio State University Comprehensive Cancer Center โ€” Columbus, Ohio
  • University of Cincinnati Cancer Center-West Chester โ€” West Chester, Ohio

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 826-4673

Email: becomingapatient@coh.org

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†—