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Clinical Trials/NCT02999984
NCT02999984
Completed
Phase 1

Efficacy and Safety of Cryopreserved Formulation of Autologous CD34+ Hematopoietic Stem Cells Transduced Ex Vivo With Elongation Factor 1 Alpha Shortened (EFS) Lentiviral Vector Encoding for Human ADA Gene in Subjects With Severe Combined Immunodeficiency Due to ADA Deficiency

University of California, Los Angeles1 site in 1 country10 target enrollmentDecember 16, 2016

Overview

Phase
Phase 1
Intervention
Infusion of autologous cryopreserved EFS-ADA LV CD34+ cells (OTL-101)
Conditions
Severe Combined Immunodeficiency Due to ADA Deficiency
Sponsor
University of California, Los Angeles
Enrollment
10
Locations
1
Primary Endpoint
Percentage of Participants With Treatment Efficacy After Treatment With OTL 101 (6 Months)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

This is a prospective, non-randomized, single-cohort, longitudinal, single-center, clinical study designed to assess the efficacy and safety of a cryopreserved formulation of OTL-101 (autologous CD34+ hematopoietic stem/progenitor cells transduced ex vivo with EFS (Elongation Factor 1α Short form) Lentiviral Vector (LV) encoding for the human ADA gene) administered to ADA-SCID subjects between the ages of 30 days and 17 years of age, who are not eligible for an Human Leukocyte Antigen (HLA) matched sibling/family donor and meeting the inclusion/exclusion criteria. The OTL-101 product is infused after a minimal interval of at least 24 hours following the completion of reduced intensity conditioning. For subjects who successfully receive the OTL-101 product, pegademase bovine (PEG-ADA) Enzyme Replacement Therapy (ERT) is discontinued at Day+30 (-3/+15) after the transplant. After their discharge from hospital, the subjects will be seen at regular intervals to review their history, perform examinations and draw blood samples to assess immunity and safety.

Registry
clinicaltrials.gov
Start Date
December 16, 2016
End Date
September 26, 2019
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Donald B. Kohn, M.D.

Principal Investigator

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • Provision of written informed consent prior to any study related procedures. In this study consent must be provided by the parents/legal guardians and, where applicable according to local laws, a signed assent from the child,
  • Subjects ≥30 days and \<18 years of age,
  • With a diagnosis of ADA-SCID based on:
  • Evidence of ADA deficiency, defined as:
  • i. Decreased ADA enzymatic activity in erythrocytes, leukocytes, skin fibroblasts, or in cultured fetal cells to levels consistent with ADA-SCID as determined by the reference laboratory, or ii. Identified mutations in ADA alleles consistent with a severe reduction in ADA activity,
  • Evidence of ADA-SCID based on either:
  • i. Family history of a first order relative with ADA deficiency and clinical and laboratory evidence of severe immunologic deficiency, or ii. Evidence of severe immunologic deficiency in subjects prior to the institution of immune restorative therapy, based on
  • Lymphopenia (absolute lymphocyte count (ALC) \<400 cells/µL) OR absence or low number of T cells (absolute CD3+ count \< 300 cells/µL), or
  • Severely decreased T lymphocyte blastogenic responses to phytohemagglutinin (either \<10% of lower limit of normal controls for the diagnostic laboratory, or \<10% of the response of the normal control of the day, or stimulation index \<10), or
  • Identification of SCID by neonatal screening revealing low T cell Receptor Excision Circle (TREC) levels.

Exclusion Criteria

  • Ineligible for autologous Hematopoietic Stem Cell Transplantation (HSCT) as per clinical site criteria.
  • Other conditions which in the opinion of the Principal Investigator and/or Co Investigators, contraindicate the harvest of bone marrow, the administration of Busulfan and the infusion of transduced cells, or which indicate an inability of the subject or subject's parent/legal guardian to comply with the protocol.
  • Hematologic abnormality, defined as:
  • Anemia (Hb \<8.0 g/dl).
  • Neutropenia (ANC \<500/mm3). Note: ANC \<500 with absence of myelodysplastic syndrome on bone marrow aspirate and biopsy and normal marrow cytogenetics are acceptable for eligibility.
  • Thrombocytopenia (platelet count \<50,000/mm3, at any age).
  • Prothrombin time or international normalized ratio (INR) and partial thromboplastin time (PTT) \>2 x upper limit of normal (ULN) (subjects with a correctable deficiency controlled on medication will not be excluded).
  • Cytogenetic abnormalities on peripheral blood or bone marrow or amniotic fluid (if available).
  • Prior allogeneic HSCT with cytoreductive conditioning.
  • Pulmonary abnormality, defined as:

Arms & Interventions

Gene Therapy

Infusion of autologous cryopreserved EFS-ADA LV CD34+ cells

Intervention: Infusion of autologous cryopreserved EFS-ADA LV CD34+ cells (OTL-101)

Gene Therapy

Infusion of autologous cryopreserved EFS-ADA LV CD34+ cells

Intervention: busulfan

Gene Therapy

Infusion of autologous cryopreserved EFS-ADA LV CD34+ cells

Intervention: PEG-ADA ERT

Outcomes

Primary Outcomes

Percentage of Participants With Treatment Efficacy After Treatment With OTL 101 (6 Months)

Time Frame: 6 months

Efficacy of OTL-101 treatment at 6 months post OTL-101 infusion based on the following parameters and thresholds: 1. ADA enzyme activity in erythrocytes above baseline/pretreatment level (i.e., \>0 units). ADA enzyme activity is measured to assess the amount of functional gene product produced from the normal ADA transgene delivered by EFS-ADA LV. 2. Absolute CD3+ T cell counts ≥200 cells/μL. Increase in CD3+ T cell counts is a marker of immune reconstitution. 3. Granulocyte samples positive for vector sequences by quantitative Polymerase Chain Reaction (PCR) (≥1/10,000 cells). Vector copy number (VCN) in the Peripheral Blood (PB) Granulocytes fraction that was T cell depleted, is a surrogate for amount of engrafted genetically modified Hematopoietic stem cell (HSC) that are producing granulocytes every 3-5 days.

Event-free Survival (EvFS) of Subjects Treated With Investigational Medicinal Product (IMP) (1 Year)

Time Frame: 12 Months

Event-free survival is defined as the percentage of subjects alive with no "event", an "event" being the resumption of PEG-ADA ERT or the need for a rescue allogeneic Hematopoietic Stem Cell Transplant (HSCT), or death.

Overall Survival (OS) of Subjects Treated With Investigational Medicinal Product (IMP) (1 Year)

Time Frame: 12 Months

Overall survival is defined as the percentage of subjects alive at 12 months post- treatment with cryopreserved OTL-101.

Secondary Outcomes

  • OS of Subjects Treated With Investigational Medicinal Product (IMP) (2 Years)(24 months)
  • Percentage of Patients Who Stopped Immunoglobulin Replacement Therapy (IgRT) (2 Years)(24 months)
  • Severe Infections Excluding First 3 Months After Treatment(24 months)
  • Change From Baseline in Quality of Life Measures (2 Years)(24 months)
  • EvFS of Subjects Treated With Investigational Medicinal Product (IMP) (2 Years)(24 months)
  • Change From Baseline in CD3+ T Cell Counts (2 Years)(24 months)
  • Time to Cessation of IgRT for Those Who Stopped (2 Years)(24 months)

Study Sites (1)

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