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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01852071
Other study ID # EFS-ADA
Secondary ID U01AI1008012P01H
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date August 2, 2013
Est. completion date August 27, 2018

Study information

Verified date August 2022
Source University of California, Los Angeles
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to assess the safety and efficacy of autologous transplantation of hematopoietic stem cells (CD34+ cells) from the bone marrow (BM) of ADA-deficient SCID infants and children following human ADA cDNA transfer by the EFS-ADA lentiviral vector. The level of gene transfer in blood cells and immune function will be measured as endpoints.


Description:

The study is open to twenty (20) infants and children diagnosed with ADA-deficient SCID who did not have a medically eligible, human leukocyte antigen (HLA)-identical sibling donor for bone marrow transplantation. The EFS-ADA lentiviral vector with the human ADA cDNA will be used to transduce autologous CD34+ cells from the bone marrow of these subjects. The subjects will receive 4 mg/kg busulfan prior to re-infusion of their gene-modified cells. Safety is the primary endpoint. During the follow-up phase, the investigators aim to determine whether the cells could engraft and produce mature cells that contain and express the corrected ADA gene in the absence of pegademase bovine (PEG-ADA) enzyme replacement therapy (ERT), which will be withheld at Day +30 following transplant. Efficacy studies to evaluate the level of immune reconstitution, will be performed in the first and second years of the study.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date August 27, 2018
Est. primary completion date August 27, 2018
Accepts healthy volunteers No
Gender All
Age group 1 Month to 17 Years
Eligibility Inclusion Criteria: -Children = 1.0 months of age with a diagnosis of ADA-deficient SCID based on A. Decreased ADA enzymatic activity in erythrocytes, leukocytes, skin fibroblasts, or in cultured fetal cells to levels consistent with ADA-deficient SCID as determined by reference laboratory or confirmed ADA gene mutation(s) known to cause disease , AND B. Evidence of severe combined immunodeficiency based on either: 1. Family history of first order relative with ADA deficiency and clinical and laboratory evidence of severe immunologic deficiency, OR 2. Evidence of severe immunologic deficiency in subject prior to institution of immune restorative therapy, based on 1. lymphopenia (absolute lymphocyte count <400 cells/mcL) OR absence or low number of T cells (absolute CD3+ count <300 cells/mcL) OR 2. severely decreased T lymphocyte blastogenic responses to phytohemagglutinin (either <10% of lower limit of normal controls for the diagnostic laboratory, <10% of the response of the normal control of the day, or stimulation index <10) - Ineligible for matched sibling allogeneic bone marrow transplantation: absence of a medically eligible HLA-identical sibling, with normal immune function, who may serve as an allogeneic bone marrow donor - Signed written informed consent according to guidelines of the Institutional Review Board (IRB) (UCLA Office of Human Research Protection Program and National Human Genome Research Institute (NHGRI) IRB Exclusion Criteria: 1. Age = 1.0 months Appropriate organ function as outlined below must be observed within 60 days of entering this trial. 2. Hematologic 1. Anemia (hemoglobin < 10.5 g/dl at < 2 years of age, or < 11.5 g/dl at > 2 years of age). 2. Neutropenia (absolute granulocyte count <500/mm3. 3. Thrombocytopenia (platelet count < 150,000/mm3, at any age). 4. International Normalised Ratio (INR) or Prothrombin Time (PT) > 2 times the upper limits of normal or Partial Thromboplastin Time (PTT) > 2.33 times the upper limit of normal (patients with a correctable deficiency controlled on medication will not be excluded). 5. Cytogenetic abnormalities on peripheral blood or bone marrow or amniotic fluid (if available). 6. Prior allogeneic Hematopoietic Stem Cell Transplant (HSCT) with cytoreductive conditioning 3. Infectious a. Evidence of infection with HIV-1, hepatitis B, Hepatitis C, or parvovirus B 19 by DNA Polymerase Chain Reaction (PCR) within 90 days prior to bone marrow harvest. If other infection is present, it must be under control (e.g. stable or decreasing viral load) at the time of screening 4. Pulmonary 1. Resting O2 saturation by pulse oximetry < 95% on room air. 2. Chest x-ray indicating active or progressive pulmonary disease. 5. Cardiac 1. Abnormal electrocardiogram (EKG) indicating cardiac pathology. 2. Uncorrected congenital cardiac malformation with clinical symptomatology. 3. Active cardiac disease, including clinical evidence of congestive heart failure, cyanosis, hypotension. 4. Poor cardiac function as evidenced by LV ejection fraction < 40% on echocardiogram. 6. Neurologic 1. Significant neurologic abnormality by examination. 2. Uncontrolled seizure disorder. 7. Renal 1. Renal insufficiency: serum creatinine >= 1.2 mg/dl, or >= 3+ proteinuria. 2. Abnormal serum sodium, potassium, calcium, magnesium, phosphate at grade III or IV by Division of AIDS Toxicity Scale. 8. Hepatic/GI: 1. Serum transaminases > 5 times the upper limit of normal (ULN). 2. Serum bilirubin > 2 times ULN. 3. Serum glucose > 1.5 times ULN. 4. Intractable severe diarrhea. 9. Oncologic 1. Evidence of active malignant disease other than dermatofibrosarcoma protuberans (DFSP) 2. Evidence of DFSP expected to require anti-neoplastic therapy within the 5 years following the infusion of genetically corrected cells 3. Evidence of DFSP expected to be life limiting within the 5 years following the infusion of genetically corrected cells 10. Known sensitivity to Busulfan 11. General 1. Expected survival < 6 months. 2. Pregnant. 3. Major congenital anomaly. 4. Ineligible for autologous HSCT by the criteria at the clinical site. 5. Other conditions which in the opinion of the principal investigator and/or co-investigators, contra-indicate the bone marrow harvest, the administration of busulfan, infusion of transduced cells or indicate the patient or patient's parents/primary caregivers inability to follow protocol.

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
Infusion of autologous EFS-ADA LV CD34+ (OTL-101)
autologous EFS-ADA LV CD34+ cells (OTL-101) are infused intravenously
Drug:
busulfan
Busulfan is used for non-myeloablative conditioning
PEG-ADA ERT
PEG-ADA ERT is discontinued at Day +30 (-3/+15 days) after successful engraftment

Locations

Country Name City State
United States Mark O. Hatfield Clinical Research Center, NIH Bethesda Maryland
United States Mattel Children's Hospital, UCLA Los Angeles California

Sponsors (5)

Lead Sponsor Collaborator
University of California, Los Angeles National Heart, Lung, and Blood Institute (NHLBI), National Human Genome Research Institute (NHGRI), National Institute of Allergy and Infectious Diseases (NIAID), Orchard Therapeutics

Country where clinical trial is conducted

United States, 

References & Publications (2)

Candotti F, Shaw KL, Muul L, Carbonaro D, Sokolic R, Choi C, Schurman SH, Garabedian E, Kesserwan C, Jagadeesh GJ, Fu PY, Gschweng E, Cooper A, Tisdale JF, Weinberg KI, Crooks GM, Kapoor N, Shah A, Abdel-Azim H, Yu XJ, Smogorzewska M, Wayne AS, Rosenblatt HM, Davis CM, Hanson C, Rishi RG, Wang X, Gjertson D, Yang OO, Balamurugan A, Bauer G, Ireland JA, Engel BC, Podsakoff GM, Hershfield MS, Blaese RM, Parkman R, Kohn DB. Gene therapy for adenosine deaminase-deficient severe combined immune deficiency: clinical comparison of retroviral vectors and treatment plans. Blood. 2012 Nov 1;120(18):3635-46. doi: 10.1182/blood-2012-02-400937. Epub 2012 Sep 11. — View Citation

Carbonaro DA, Zhang L, Jin X, Montiel-Equihua C, Geiger S, Carmo M, Cooper A, Fairbanks L, Kaufman ML, Sebire NJ, Hollis RP, Blundell MP, Senadheera S, Fu PY, Sahaghian A, Chan RY, Wang X, Cornetta K, Thrasher AJ, Kohn DB, Gaspar HB. Preclinical demonstration of lentiviral vector-mediated correction of immunological and metabolic abnormalities in models of adenosine deaminase deficiency. Mol Ther. 2014 Mar;22(3):607-622. doi: 10.1038/mt.2013.265. Epub 2013 Nov 20. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Survival (OS) of Subjects Treated With Investigational Medicinal Product (IMP) (1 Year) Overall survival is defined as the percentage of subjects alive at 12 months post- treatment with OTL-101 or HSCT 12 months
Primary Event-free Survival (EvFS) of Subjects Treated With Investigational Medicinal Product (IMP) (1 Year) 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. 12 months
Secondary OS of Subjects Treated With Investigational Medicinal Product (IMP) (2 Years) OS is defined as the percentage of subjects alive at 24 months post- treatment with OTL-101 or HSCT 24 months
Secondary EvFS of Subjects Treated With Investigational Medicinal Product (IMP) (2 Years) 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 allogenic Hematopoietic Stem Cell Transplant (HSCT), or death. 24 months
Secondary Vector Copy Number (VCN) in Peripheral Blood (PB) Granulocytes. Vector copy number in the PB granulocyte 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. VCN analysis was performed by Droplet Digital PCR (ddPCR) on DNA extracted from peripheral blood granulocytes. 24 months
Secondary VCN in Peripheral Blood Mononuclear Cells (PBMCs) PBMC VCN is a measure of the accumulation of peripheral blood leukocytes arising from engrafted, genetically modified HSC. VCN analysis was performed by ddPCR on DNA extracted from PBMC. 24 months
Secondary ADA Activity in Erythrocytes ADA enzyme activity measured to assess the amount of functional gene product produced from the normal ADA transgene delivered by EFS-ADA LV; persistence of ADA enzyme activity over time demonstrates successful engraftment and differentiation of genetically modified HSC. 24 months
Secondary Reduction in Deoxyadenosine Nucleotide (dAXP) in Erythrocytes Decreased dAXP levels coincide with increased ADA enzyme activity, detoxification was used to demonstrate functional ADA enzyme production from the introduced ADA transgene. The threshold for detoxification was <100 µmol/L. 24 months
Secondary Change From Baseline in CD3+ T Cell Counts (2 Years) Immune reconstitution was assessed by change in CD3+ T Cell counts at baseline to Month 24. 24 months
Secondary Number of Single Integration Sites Representing >30% of the Total Integration Sites (2 Years) Vector Integration Site Analysis (VISA) allowed determination of the distribution of vector integration sites in each subject's genome, as well as the relative clonal abundance. VISA was to be considered abnormal for a subject if, in 2 or more instances during the course of follow-up, a single integration site was found to represent >30% of the total integration sites detected. 24 months
Secondary Severe Infection Rate Excluding the First Three Months After Treatment The infections of interest in this study were severe infections or opportunistic infectious episodes, defined as infections requiring hospitalization or prolonging hospitalization and/or documented infections by opportunistic pathogens. Infections that took place in the first 3 months of follow-up post treatment were excluded from calculations to avoid possible bias introduced in the data by the effects of conditioning. 24 months
See also
  Status Clinical Trial Phase
Enrolling by invitation NCT01346150 - Patients Treated for SCID (1968-Present)
Completed NCT01420627 - EZN-2279 in Patients With ADA-SCID Phase 3
Completed NCT02022696 - Treatment of SCID Due to ADA Deficiency With Autologous Transplantation of Cord Blood or Hematopoietic CD 34+ Cells After Addition of a Normal Human ADA cDNA by the EFS-ADA Lentiviral Vector Phase 1
Withdrawn NCT01182857 - Quality of Life and Neuropsychiatric Sequelae in Patients Treated With Gene Therapy for ADA-SCID and in Their Parents