An Intermediate Expanded Use Trial of DFMO

Sponsor: Giselle Sholler

Expanded Access
Sponsor score: 60
Inactive

ClinicalTrials ID:NCT03581240

Provider View

This trial provides DFMO to subjects aged 0-30 with relapsed rare tumors showing increased LIN28 expression, MYCN amplification, or ornithine decarboxylase upregulation. Eligible participants must have completed standard therapies and meet specific criteria. DFMO is administered orally, with doses adjusted for CNS involvement. Participants must not be on other investigational drugs.

Patient Parameters

Program Overview

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.

Eligibility Criteria

Inclusion Criteria

  • 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:

    1. High risk neuroblastoma patients that have completed standard of care upfront therapy and are not eligible for NMTRC014.
    2. Medulloblastoma patients who have completed standard of care therapies.
    3. Relapsed/refractory neuroblastoma patients who have completed standard of care therapies.
    4. 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

Exclusion Criteria

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

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