Trial record 6 of 29 for:    "Wiskott Aldrich syndrome"

Pilot and Feasibility Study of Hematopoietic Stem Cell Gene Transfer for the Wiskott-Aldrich Syndrome

This study is currently recruiting participants. (see Contacts and Locations)
Verified July 2014 by Children's Hospital Boston
Sponsor:
Information provided by (Responsible Party):
Children's Hospital Boston
ClinicalTrials.gov Identifier:
NCT01410825
First received: August 4, 2011
Last updated: July 23, 2014
Last verified: July 2014
  Purpose

The Wiskott-Aldrich Syndrome (WAS) is an inherited disorder that results in defects of the blood and bone marrow. It affects boys because the genetic mistake is carried on the X chromosome. Normal people have blood cells called platelets that stop bleeding when blood vessels are damaged. Boys with WAS have low numbers of platelets that do not function correctly. Boys with WAS are thus at risk for severe life-threatening bleeding. A normal immune system is made of special blood cells called white blood cells, which protect against infection and also fight certain types of cancer. In WAS, these white blood cells don't work as well as they should, making these boys very susceptible to infections and to a form of blood cancer known as lymphoma. The abnormal white blood cells of patients with WAS also cause diseases such as eczema and arthritis. Although WAS can be mild, severe forms need treatment as early as possible to prevent life-threatening complications due to bleeding, infection and blood cancer.

Over the past decade, investigators have developed new treatments based on the investigators knowledge of the defective gene causing WAS. The investigators can now use genes as a type of medicine that will correct the problem in the patient's own bone marrow. The investigators call this process gene transfer. The procedure is very similar to a normal bone marrow transplant, in that the old marrow is killed off using chemotherapy, but is different because the patient's own bone marrow is given back after it is treated by gene transfer. This approach can be used even if the patient does not have any matched donors available and will avoid problems such as GVHD and rejection. The investigators wish to test whether this approach is safe and whether gene transfer will lead to the development of a healthy immune and blood system.


Condition Intervention Phase
Wiskott-Aldrich Syndrome
Biological: Retrovirus-mediated gene transfer
Phase 1
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Pilot and Feasibility Study of Hematopoietic Stem Cell Gene Transfer for the Wiskott-Aldrich Syndrome

Resource links provided by NLM:


Further study details as provided by Children's Hospital Boston:

Primary Outcome Measures:
  • Safety of infusion of transduced cells [ Time Frame: 5 Years ] [ Designated as safety issue: Yes ]
    Safety of infusion of transduced cells as rescue of hematopoiesis after conditioning (hematopoietic recovery as assessed by absolute neutrophil count (ANC) above 0.5 x 109 /l for three consecutive days, achieved within 6 weeks following infusion).

  • Engraftment of genetically corrected T cells [ Time Frame: 5 Years ] [ Designated as safety issue: Yes ]
    Engraftment of genetically corrected T cells in peripheral blood (as assessed by evidence of vector sequences in >1% of CD3+ T cells) at 6 months.


Estimated Enrollment: 5
Study Start Date: July 2011
Estimated Study Completion Date: July 2031
Estimated Primary Completion Date: July 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Gene transfer
Open label single arm study
Biological: Retrovirus-mediated gene transfer
Two procedures: 1) Bone marrow harvest from the patient's posterior iliac crests or collection of peripheral blood stem cells via apheresis procedure. 2) One time infusion of patient's transduced bone marrow cells.

Detailed Description:

Wiskott-Aldrich syndrome (WAS) (OMIM 301000) is a rare X-linked immunodeficiency caused by mutations in a single gene, WAS, mapping to Xp11.22-Xp11.3 and coding for the Wiskott-Aldrich Syndrome Protein (WASP) 1. WASP is a critical regulator of actin signaling with expression limited to hematopoietic cells, and thus is required for multiple functions including T cell activation, dendritic cell migration and podosome formation, and B cell terminal development and function. WAS is characterized by microthrombocytopenia, recurrent infections, eczema and associated with a high incidence of auto-immunity and of lymphoid malignancies. Classic or severe WAS, is generally observed in patients with nonsense mutations or insertions/deletions resulting in frameshift or splice-site mutations or missense mutations and resulting in unstable protein 2. With few exceptions, WASP-negative patients have classical disease. Affected patients have a severely reduced life expectancy.

Currently, the only curative option for WAS patients is hematopoietic stem cell transplantation (HSCT). This treatment is most successful when an HLA-identical sibling or matched unrelated donor is available and results in correction of microthrombocytopenia and immune dysfunction, even when stable mixed chimerism occurs. However, even patients undergoing matched HSCT can suffer from considerable morbidity and mortality due to graft versus host disease (GVHD) and many patients lack an HLA-identical donor. The outcome of mismatched related HSCT is consistently poor with survival of approximately 50%. Gene transfer is an attractive alternative treatment for WAS. Successful gene transfer using autologous gene-corrected HSC would overcome clinical complications linked to GVHD and its treatment. Furthermore, in contrast to allogeneic HSCT, gene transfer would not be limited by the availability of compatible donors. Several lines of evidence indicate that partial reconstitution with gene corrected cells may be sufficient to ameliorate the disease.

We propose here a Pilot and Feasibility study of ex vivo gene transfer using a lentiviral vector (LV) to transduce autologous bone marrow derived CD34+ HSC. Cells will be infused into patients conditioned with cytoreductive chemotherapy. Our collaborating investigators in Europe have developed a LV encoding the human WAS cDNA under control of the WAS promoter and pseudotyped with the Vesicular Stomatitis Virus glycoprotein (VSVg) envelope. This w1.6_hWASP_WPRE (VSVg) LV (abbreviated as w1.6W) has been shown to be efficacious in both in vitro and in vivo preclinical models. Safety including cellular toxicity, insertional mutagenesis and tumor formation has been studied by a number of methods including: 1) a sensitive in vitro transformation assay, 2) toxicity studies in transduced human CD34+ cells, 3) examination of the insertional pattern in transduced murine cells, and 4) long-term observation and secondary transplant studies in mice. In the United States, we plan to enroll 5 boys with classic WAS who lack a matched related or unrelated donor. Parallel studies (not under our Investigational New Drug application) using the same LV produced in the same facility, Genethon, will be conducted in London, UK (5 subjects) and Paris, France (5 subjects). The primary objective will be to demonstrate feasibility and safety. The secondary objective will be to assess therapeutic efficacy.

  Eligibility

Ages Eligible for Study:   3 Months to 35 Years
Genders Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Confirmed molecular diagnosis by DNA sequencing and either

    1. absence of the WAS protein by flow cytometry OR
    2. clinical score 3-5
  2. Age 3 months to 35 years
  3. For subjects < 5 years of age:

    1. Lack of HLA-genotypically identical bone marrow donor.
    2. Lack of a 9/10 or 10/10 molecularly HLA-matched unrelated donor after 3 months of searching.
    3. Lack of a 6/6 molecularly HLA-matched cord blood donor of adequate cell number after 3 months of searching
  4. For subjects 5 years of age or older:

    a.Lack of HLA-genotypically identical bone marrow donor.

  5. Subjects who have undergone allogeneic transplant previously must additionally have:

    1. Failure defined as <5% donor T cell engraftment and
    2. Contraindication to re-use of the same donor due to severe GVHD or non-availability.
  6. Parental/guardian/patient signed informed consent
  7. Willingness to return for follow-up during the 5 year study period.
  8. Adequate organ function and performance status

    1. Performance status ≥50% (Lansky play for age <16 years, Karnofsky for age ≥16 years)
    2. Left ventricular ejection fraction >40% or shortening fraction >25%
    3. Bilirubin ≤ 2.0 mg/dL
    4. Measured creatinine clearance or GFR by nuclear medicine study ≥40 ml/min/1.73 m2
    5. DLCO (corrected for hemoglobin), FEV1, FVC >50% of predicted; if age < 7 years, then oxygen saturation >92% on room air

Exclusion Criteria:

  1. Contraindication to bone marrow harvest, or to administration of conditioning medication.
  2. Known positive HIV serology or HIV nucleic acid testing.
  3. Other uncontrolled infection.
  4. Active malignancy other than EBV lymphoproliferative disease.
  5. Known myelodysplasia of the bone marrow or abnormal bone marrow cytogenetics
  6. Congenital cardiac disease with congestive heart failure
  7. Oxygen dependence at baseline
  8. Any other condition that, in the opinion of the Investigator, may compromise the safety or compliance of the patient or would preclude the patient from successful study completion. This may include but is not limited to:

    • Severe deterioration of clinical condition after collection of cells but before infusion of transduced cells
    • Documented refusal or inability of the family to return for scheduled visits
    • Other concerns about unwillingness or inability to comply with protocol requirements
    • Unforeseen rare circumstances such as sudden loss of legal guardianship
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01410825

Contacts
Contact: David A Williams, M.D. 617-919-2777 DAWilliams@tch.harvard.edu
Contact: Colleen H. Dansereau, RN 617-919-7008 colleen.dansereau@childrens.harvard.edu

Locations
United States, Massachusetts
Children's Hospital Boston Recruiting
Boston, Massachusetts, United States, 02116
Contact: Sung-Yun Pai, MD    617-919-2508    Sung-Yun.Pai@Childrens.Harvard.edu   
Contact: Luigi Notarangelo, M.D.    617-919-2276    Luigi.Notarangelo@Childrens.Harvard.edu   
Sponsors and Collaborators
Children's Hospital Boston
Investigators
Principal Investigator: Sung-Yun Pai, M.D. Children's Hospital Boston
  More Information

No publications provided

Responsible Party: Children's Hospital Boston
ClinicalTrials.gov Identifier: NCT01410825     History of Changes
Other Study ID Numbers: CHB-P00000148
Study First Received: August 4, 2011
Last Updated: July 23, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Children's Hospital Boston:
WAS
Wiskott
Gene Transfer
Gene Therapy

Additional relevant MeSH terms:
Wiskott-Aldrich Syndrome
Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders
Hematologic Diseases
Hemorrhagic Disorders
Lymphopenia
Leukopenia
Leukocyte Disorders
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Immunologic Deficiency Syndromes
Immune System Diseases

ClinicalTrials.gov processed this record on July 29, 2014