Status:

ACTIVE_NOT_RECRUITING

Lentiviral-mediated Gene Therapy for Pediatric Patients With Fanconi Anemia Subtype A

Lead Sponsor:

Rocket Pharmaceuticals Inc.

Conditions:

Fanconi Anemia Complementation Group A

Eligibility:

All Genders

1-17 years

Phase:

PHASE2

Brief Summary

This is an open-label Phase II clinical trial to evaluate the efficacy of a hematopoietic cell-based gene therapy for pediatric patients with Fanconi Anemia, subtype A (FA-A). Hematopoietic stem cell...

Detailed Description

This is a pediatric open-label Phase II clinical trial to assess the efficacy of a hematopoietic gene therapy consisting of autologous CD34+ enriched cells transduced with a lentiviral vector carrying...

Eligibility Criteria

Inclusion

  • Fanconi anemia as diagnosed by chromosomal fragility assay of cultured lymphocytes in the presence of diepoxybutane (DEB) or similar DNA-crosslinking agent
  • Patient of the complementation group FA-A
  • Minimum age: 1 year and minimum weight of 8 kg.
  • Maximum age: 17 years
  • At least 30 CD34+ cells/µL are determined in one BM aspiration within 3 months prior to the CD34+ cell collection.
  • Provide informed consent in accordance with current legislation
  • Women of childbearing age must have a negative urine pregnancy test at the baseline visit, and accept the use of an effective contraception method during participation in the trial

Exclusion

  • Patients with an available and medically eligible human leukocyte antigen (HLA)-identical sibling donor
  • Evidence of myelodysplastic syndrome or leukemia, or cytogenetic abnormalities other than those predictive of these conditions in bone marrow (BM) aspirate analysis. This assessment should be made by valid studies conducted within the 3 months before the patient enters the clinical trial
  • Patients with somatic mosaicism associated with stable or improved counts in all PB cell lineages (If T-lymphocyte chromosomal fragility analysis indicates potential mosaicism, a medically significant decrease in at least one blood lineage over time must be documented to enable eligibility)
  • Lansky performance index ≤ 60%
  • Any concomitant disease or condition that, in the opinion of the Principal Investigator, deems the patient unfit to participate in the trial
  • Pre-existing sensory or motor impairment \>/= grade 2 according to the criteria of the National Cancer Institute (NCI)
  • Pregnant or breastfeeding women
  • Hepatic dysfunction as defined by either:
  • Bilirubin \> 3 x the upper limit of normal (ULN)
  • Alanine aminotransferase (ALT ) \> 5 x ULN
  • Aspartate aminotransferase (AST) \> 5 x ULN For subjects with bilirubin, ALT, or AST above ULN, a workup to identify the etiology of liver abnormality should be conducted prior to confirmation of eligibility as stipulated in exclusion criterion 5, including evaluation of viral hepatitis, iron overload, drug injury or other causes.
  • Renal dysfunction requiring either hemodialysis or peritoneal dialysis
  • Pulmonary dysfunction as defined by either:
  • Need for supplemental oxygen during the prior 2 weeks (in absence of acute infection)
  • Oxygen saturation (by pulse oximetry) \<90%
  • Evidence of active metastatic or locoregionally advanced malignancy for which survival is anticipated to be less than 3 years
  • Subject is receiving androgens (i.e. danazol, oxymetholone)
  • Subject is receiving other investigational therapy for treatment/prevention of FA-associated bone marrow failure

Key Trial Info

Start Date :

November 28 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2025

Estimated Enrollment :

7 Patients enrolled

Trial Details

Trial ID

NCT04069533

Start Date

November 28 2019

End Date

February 1 2025

Last Update

May 22 2024

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Hospital Infantil Universitario Niño Jesús (HIUNJ)

Madrid, Spain, 28009

2

University College London Great Ormond Street Institute of Child Health (GOSH)

London, United Kingdom, WC1N 1EH