๐๏ธ Verified NIH Record โข Updated 2026-08-25
Digoxin Medulloblastoma Study (NCT06701812)
Evaluation of Digoxin for Relapsed Non-WNT, Non-SHH Medulloblastoma
๐ข Recruiting Phase2 ๐ Investigational Drug / Biologic Sponsor: H. Lee Moffitt Cancer Center and Research Institute
๐ฉบ Plain-English Summary (8th-Grade Level)
The purpose of this study is to evaluate the efficacy of digoxin in treating relapsed non-SHH, non-WNT medulloblastoma in pediatric and young adult patients.
Who can join: Review the eligibility criteria below.
Location: University of Alabama at Birmingham Children's of Alabama โ Birmingham, Alabama
Age range: 12 Months to 30 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (17 Sites)
- University of Alabama at Birmingham Children's of Alabama โ Birmingham, Alabama
- Phoenix Childrens Hospital โ Phoenix, Arizona
- Arkansas Childrens Hospital โ Little Rock, Arkansas
- Connecticut Children's Medical Center โ Hartford, Connecticut
- Children's National Medical Center โ Washington D.C., District of Columbia
- Nemours Jacksonville โ Jacksonville, Florida
- University of Miami โ Miami, Florida
- Johns Hopkins All Children's โ St. Petersburg, Florida
- St. Joseph's Children's Hospital โ Tampa, Florida
- University of Kentucky โ Lexington, Kentucky
- Johns Hopkins Sidney Kimmel Comprehensive Cancer Center โ Baltimore, Maryland
- Washington University St. Louis โ St Louis, Missouri
- Montefiore Medical Center โ The Bronx, New York
- UNC Lineberger Comprehensive Cancer Center โ Chapel Hill, North Carolina
- Levine Cancer Institute โ Charlotte, North Carolina
- Vanderbilt University Medical Center โ Nashville, Tennessee
- UT Southwestern โ Dallas, Texas
๐ Contact the Study Coordinator
Phone: (813) 745-6250
Email: Jessica.Crimella@moffitt.org
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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.
More studies in Medulloblastoma
- Reduced Craniospinal Radiation Therapy and Chemotherapy in Treating Younger Patients With Newly Diagnosed WNT-Driven Medulloblastoma โ Birmingham, Alabama
- A Clinical and Molecular Risk-Directed Therapy for Newly Diagnosed Medulloblastoma โ Palo Alto, California
- A Pilot Study of SurVaxM in Children Progressive or Relapsed Medulloblastoma, High Grade Glioma, Ependymoma and Newly Diagnosed Diffuse Intrinsic Pontine Glioma โ Los Angeles, California
- HeadStart4: Newly Diagnosed Children (<10 y/o) With Medulloblastoma and Other CNS Embryonal Tumors โ Birmingham, Alabama
- Comparison of Neurocognitive Outcome in Two Standard Regimen for Treatment of Low-risk Medulloblastoma โ Birmingham, Alabama
- Liothyronine in Combination With BIT Regimen for Medulloblastoma With or Without Minimal Residual Disease โ San Francisco, California
Explore by condition: All Medulloblastoma clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.