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Clinical Trials/NCT01906541
NCT01906541
Unknown
Phase 1

A Phase I/II Gene Therapy Trial for X-CGD With a SIN Gammaretroviral Vector

Hubert Serve, Prof., MD1 site in 1 country5 target enrollmentJuly 2013

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
X-linked Chronic Granulomatous Disease
Sponsor
Hubert Serve, Prof., MD
Enrollment
5
Locations
1
Primary Endpoint
Transduction rate of granulocyte colony-stimulating factor (G-CSF) mobilized peripheral CD34+ cells from CGD patients with a SIN gamma retroviral vector
Last Updated
12 years ago

Overview

Brief Summary

X-linked chronic granulomatous disease (X-CGD) is a rare inherited immune defect, which is caused by the inability of phagocytic cells to produce reactive oxygen species due to a defect in the gp91phox subunit of the NADPH oxidase complex. X-CGD patients suffer from recurrent and life-threatening infections and severe hyperinflammatory complications.

The only curative treatment for X-CGD is allogenic hematopoietic stem cell transplantation, but this procedure implies severe risks and many patients lack an appropriate donor. Therefore alternative curative approaches are urgently needed. In this study, patients will be treated with gene-corrected autologous CD34+ cells, using a SIN gammaretroviral vector for ex-vivo gene-therapy.

Registry
clinicaltrials.gov
Start Date
July 2013
End Date
December 2019
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Hubert Serve, Prof., MD
Responsible Party
Sponsor Investigator
Principal Investigator

Hubert Serve, Prof., MD

Head of Medical Department II

Johann Wolfgang Goethe University Hospital

Eligibility Criteria

Inclusion Criteria

  • Verified diagnosis of the X-linked form of chronic granulomatous disease, with loss of gp91phox expression (Western Blot). Evidence of less than 5% of normal oxidase production in circulating neutrophil granulocytes as measured by dihydrorhodamine- (DHR-) and nitro blue tetrazolium- (NBT-) assay
  • History of severe chronic infections with life-threatening course or severe steroid- sensitive or steroid insensitive granulomatous disease, with necessity of inpatient treatment, without sustained improvement even under maximum conservative treatment measures
  • No Human Leukocyte Antigen (HLA) identical (10/10 match) sibling- or unrelated donor, or contraindications for allogenic stem cell transplantation in presence of a suitable donor. The lack of an HLA-identical (10/10 match) sibling- or unrelated donor has to be confirmed by an unsuccessful search in national and international donor registers for at leat 3 months
  • Normal organ-function: glomerular filtration rate (GFR) ≥ 60ml/min., Bilirubin ≤ 1.5-fold upper reference-level, normal parameters for liver enzymes and clotting (TPZ 75-100%, partial thromboplastin time (PTT) 30-38sec, Fibrinogen 200-400mg/dl), Leukocytes \> 3 x 10\^9/l, Granulocytes \> 1.5 x 10\^9/l, Thrombocytes \>100 x 10\^9/l
  • Contraception from start of G-CSF application until 1 year after retransfusion of the gene-corrected cells
  • No interferon-gamma injection within two weeks prior to hematopoietic stem cell mobilization
  • Karnofsky-Index \> 70%
  • Signed informed consent

Exclusion Criteria

  • Patients with non-controlled acute infections
  • Severe cardiac or pulmonary malfunctions: ejection fraction \< 60%, valvular heart disease \> II°, arrhythmia requiring therapy, forced expiratory volume at one second/vital capacity (FEV1/VC) \< 75% , diffusion capacity of lung for carbon monoxide (DLCO) \<60%
  • Bilirubin \> 1.5-fold upper reference-level
  • HIV-, Hepatitis B- or C - infection
  • Contraindications for G-CSF administration, as autoimmune vasculitis.
  • Contraindications for stem cell apheresis, as low hemoglobin \< 8g/dl, cardiovascular instability or severe coagulopathy
  • Pregnancy or breast-feeding
  • Drug- or alcohol-abuse
  • Lack of search for an unrelated donor
  • Patients with a HLA 9/10 mismatched unrelated donor (MMUD) will be excluded, if a thorough risk-benefit analysis favors allogenic hematopoietic stem cell transplantation (HSCT)

Outcomes

Primary Outcomes

Transduction rate of granulocyte colony-stimulating factor (G-CSF) mobilized peripheral CD34+ cells from CGD patients with a SIN gamma retroviral vector

Time Frame: 1 week

Engraftment rate of the transduced CD34+ cells in the patients

Time Frame: 5 years

Long-term expression of the transgene (rate of gp91phox positive cells) in circulating cells in the peripheral blood

Time Frame: 5 years

Functional reconstitution of the NADPH oxidase in circulating cells of the peripheral blood (% DHR positive cells)

Time Frame: 5 years

Frequency and severity of unexpected toxic adverse events during and after infusion of the genetically modified CD34+ cells

Time Frame: 5 years

Secondary Outcomes

  • Frequency of infections as indicator for the clinical benefit for the patients(5 years)
  • Proliferation rate of CD34+ cells in ex-vivo culture under serum-free conditions(up to 3 weeks)
  • Differentiation rate of CD34+ cells (as measured by flow cytometry) in ex-vivo culture under serum-free conditions(up to 3 weeks)
  • Transduction rate of CD34+ cells in ex-vivo culture under serum-free conditions(up to 12 weeks)

Study Sites (1)

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