NCT03581240

Brief Summary

To provide DFMO in an expanded use setting to subjects with relapsed rare tumors with increased LIN28 expression or MYCN amplification or up regulation of ornithine decarboxylase.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 26, 2018

Completed
14 days until next milestone

First Posted

Study publicly available on registry

July 10, 2018

Completed
Last Updated

February 20, 2026

Status Verified

February 1, 2026

First QC Date

June 26, 2018

Last Update Submit

February 18, 2026

Conditions

Interventions

In this study subjects without CNS disease will receive oral difluoromethylornithine (DFMO) at a dose of 500 to 1000 mg/m2 BID Subjects with CNS disease will receive a dose of 2500 mg/m2/dose BID in order to facilitate crossing into the CNS.

Also known as: DFMO

Eligibility Criteria

Age0 Years - 30 Years
Sexall
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Age: 0-30 years at the time of initial diagnosis.
  • Diagnosis: Histologic verification at either the time of original diagnosis or a previous relapse of High Risk neuroblastoma, medulloblastoma, atypical teratoid rhabdoid tumor, embryonal tumor with abundant neuropil and true rosettes, ependymoblastoma, medulloepithelioma and other rare pediatric MYC, ODC or LIN28/Let7 driven tumors (each type will form a new subset).
  • Disease Status: Subjects must be in one of the following disease categories:
  • High risk neuroblastoma patients that have completed standard of care upfront therapy and are not eligible for NMTRC014.
  • Medulloblastoma patients who have completed standard of care therapies.
  • Relapsed/refractory neuroblastoma patients who have completed standard of care therapies.
  • Rare tumors with increased LIN28 expression or MYCN amplification or up regulation of ornithine decarboxylase who have completed standard of care therapies.
  • Subjects are not eligible to enroll on DFMO studies NMTRC002, NMTRC003, NMTRC010, or NMTRC014.
  • A negative serum or urine pregnancy test is required for female subjects of child bearing potential (onset of menses or ≥13 years of age).
  • Both male and female post-pubertal study subjects need to agree to use one of the more effective birth control methods during treatment and for six months after treatment is stopped. These methods include total abstinence (no sex), oral contraceptives ("the pill"), an intrauterine device (IUD), levonorgestrol implants (Norplant), or medroxyprogesterone acetate injections (Depo-provera shots). If one of these cannot be used, contraceptive foam with a condom is recommended.
  • Informed Consent: All subjects and/or legal guardians must sign informed written consent. Assent, when appropriate, will be obtained according to institutional guidelines

You may not qualify if:

  • BSA (m2) of \<0.25
  • Investigational Drugs: Subjects who are currently receiving another investigational drug are excluded from participation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Penn State Milton S. Hershey Medical Center and Children's Hospital

Hershey, Pennsylvania, 17033, United States

AVAILABLE

Related Links

MeSH Terms

Conditions

NeuroblastomaMedulloblastomaTypical Teratoid Rhabdoid TumorNeuroectodermal Tumors, Primitive

Interventions

Eflornithine

Condition Hierarchy (Ancestors)

Neuroectodermal Tumors, Primitive, PeripheralNeoplasms, NeuroepithelialNeuroectodermal TumorsNeoplasms, Germ Cell and EmbryonalNeoplasms by Histologic TypeNeoplasmsNeoplasms, Glandular and EpithelialNeoplasms, Nerve TissueGlioma

Intervention Hierarchy (Ancestors)

OrnithineAmino Acids, BasicAmino AcidsAmino Acids, Peptides, and ProteinsAmino Acids, Diamino

Study Officials

  • Giselle Sholler, MD

    Beat Childhood Cancer

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
expanded access
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Study Chair

Study Record Dates

First Submitted

June 26, 2018

First Posted

July 10, 2018

Last Updated

February 20, 2026

Record last verified: 2026-02

Locations