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Digoxin Medulloblastoma Study
NCT06701812 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG Digoxin
Study Locations (15)
Florida
- Nemours Jacksonville — Jacksonville
- University of Miami — Miami
- Johns Hopkins All Children's — St. Petersburg
- St. Joseph's Children's Hospital — Tampa
North Carolina
- UNC Lineberger Comprehensive Cancer Center — Chapel Hill
- Levine Cancer Institute — Charlotte
Alabama
- University of Alabama at Birmingham Children's of Alabama — Birmingham
Arkansas
- Arkansas Childrens Hospital — Little Rock
Connecticut
- Connecticut Children's Medical Center — Hartford
District of Columbia
- Children's National Medical Center — Washington D.C.
Maryland
- Johns Hopkins Sidney Kimmel Comprehensive Cancer Center — Baltimore
Missouri
- Washington University St. Louis — St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2026-01-15 |
| Est. Completion | 2027-02 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06701812
The ClinicalTrials.gov registry entry for NCT06701812 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is H. Lee Moffitt Cancer Center and Research Institute, which has 562 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Medulloblastoma appearing as the primary indexed condition, and to 1 intervention — of which Digoxin is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06701812 reports 15 study locations spanning 11 distinct geographic areas — top geographies include Florida, North Carolina, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06701812 about?
NCT06701812 is a clinical study titled "Digoxin Medulloblastoma Study". 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.
What is the current status of trial NCT06701812?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 23 participants. The study started on 2026-01-15. Estimated completion is 2027-02.
What conditions does trial NCT06701812 study?
This clinical trial studies the following conditions: Medulloblastoma, Medulloblastoma, Non-WNT/Non-SHH. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06701812?
The interventions under investigation include: Digoxin (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06701812?
This trial is sponsored by H. Lee Moffitt Cancer Center and Research Institute, which has 562 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06701812 being conducted?
This trial has 15 study locations across Alabama, Arkansas, Connecticut, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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