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RECRUITING Phase 2

Eflornithine (DFMO) and Etoposide for Relapsed/Refractory Neuroblastoma

NCT04301843 · View on ClinicalTrials.gov ↗

Study Summary

Difluoromethylornithine (DFMO) will be used in an open label, multicenter, study in combination with etoposide for subjects with relapsed/refractory neuroblastoma.

Conditions Studied

Interventions

  • DRUG Eflornithine

Study Locations (20)

California

  • UCSF Benioff Children's Hospital Oakland — Oakland
  • Rady Children's Hospital — San Diego

Florida

  • Arnold Palmer Hospital for Children — Orlando
  • St. Joseph's Children's Hospital — Tampa

Missouri

  • Children's Mercy Hospitals and Clinics — Kansas City
  • Cardinal Glennon Children's Hospital — St Louis

Alabama

  • University of Alabama/Children's of Alabama — Birmingham

Arkansas

  • Arkansas Children's Hospital — Little Rock

Connecticut

  • Connecticut Children's Hospital — Hartford

Georgia

  • Augusta University Health — Augusta

Iowa

  • University of Iowa — Iowa City

Trial Details

FieldValue
Enrollment Target 131 participants
Start Date 2020-09-25
Est. Completion 2033-10-01
Phase Phase 2

Sponsor

Giselle Sholler

65 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04301843

The ClinicalTrials.gov registry entry for NCT04301843 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 131 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Giselle Sholler, which has 65 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Neuroblastoma appearing as the primary indexed condition, and to 1 intervention — of which Eflornithine 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: NCT04301843 reports 20 study locations spanning 17 distinct geographic areas — top geographies include California, Florida, Missouri. 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 NCT04301843 about?

NCT04301843 is a clinical study titled "Eflornithine (DFMO) and Etoposide for Relapsed/Refractory Neuroblastoma". Difluoromethylornithine (DFMO) will be used in an open label, multicenter, study in combination with etoposide for subjects with relapsed/refractory neuroblastoma.

What is the current status of trial NCT04301843?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 131 participants. The study started on 2020-09-25. Estimated completion is 2033-10-01.

What conditions does trial NCT04301843 study?

This clinical trial studies the following conditions: Neuroblastoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04301843?

The interventions under investigation include: Eflornithine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04301843?

This trial is sponsored by Giselle Sholler, which has 65 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04301843 being conducted?

This trial has 20 study locations across Alabama, Arkansas, California, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial