Status:
ACTIVE_NOT_RECRUITING
Gene Therapy Trial for Platelet Derived Factor VIII Production in Hemophilia A
Lead Sponsor:
Medical College of Wisconsin
Conditions:
Hemophilia A
Eligibility:
MALE
18+ years
Phase:
PHASE1
Brief Summary
This is a Phase I study. This research study is being conducted to find new ways to treat severe hemophilia A. This study is a gene therapy study. Gene therapy is an experimental way to introduce, int...
Detailed Description
This is an open label, nonrandomized, single center, phase I cohort study, involving reduced intensity conditioning, followed by a single infusion of autologous CD34+PBSC, transduced with a lentiviral...
Eligibility Criteria
Inclusion
- Study population will include: adult males \>18 years of age with a diagnosis of severe hemophilia A and currently active or a history of FVIII inhibitors (≥0.6 BU). Females will be excluded because hemophilia A is an X-linked disorder that is extremely rare in females.
- Confirmed diagnosis of severe hemophilia A by undetectable plasma factor VIII:C by a one-stage PTT-based assay and coatest chromogenic factor VIII assay. Subjects with currently active or a history of positive FVIII inhibitor titers (≥0.6 BU) irrespective of their titer or current inhibitor status will be included for enrollment.
- Subject may be prescribed prophylactic therapy with factor VIII bypassing agents or factor VIII mimetics prior to referral for inclusion in the study.
- Subjects who are treated on demand using factor VIII bypassing agents must have a history of four or more bleeding episodes requiring treatment in the six-month period prior to referral for inclusion in the study.
- Adequate bone marrow reserve as demonstrated by ANC \>1.5/cu.mm; Hemoglobin \>9g/dL; Platelets \>100,000/microliter.
- Adequate renal function, defined as creatinine clearance\>60 ml/min (Cockroft-Gault formula)
- Adequate liver function, defined as defined as total bilirubin ≤1.5 times the upper limit of normal (ULN) (excluding Gilbert's syndrome), both AST and ALT ≤3 times ULN at the time of screening, and no clinical signs or known laboratory/radiographic evidence consistent with cirrhosis.
- Subject must sign an informed consent after explanation of the study and having questions answered.
- Subject must be willing and able to document type of bleeding episodes and treatment in a paper or electronic diary during the study.
- Subject must be willing to return for regular follow-up visits during the 15-year study.
Exclusion
- A potential subject who meets any of the following exclusion criteria is ineligible to participate in the study.
- Therapy with factor VIII with the intent of immune tolerance induction within 30 days prior to inclusion within the study.
- Enrollment in another interventional clinical trial within 60 days prior to study inclusion.
- Medical contraindication to PBSC cytokine mobilization, use of GCSF, PBSC apheresis procedure or conditioning regimen.
- Medically significant organ dysfunction that would prevent compliance with conditioning or would severely limit the probability of survival based on clinical status.
- Those with a known co-existing clinically significant thrombophilic disorder, or as determined by the presence of any of the below identified on screening laboratory assessments:
- FV Leiden
- Protein S deficiency
- Protein C deficiency
- Prothrombin mutation (G20210A)
- D-dimer \>3 x the upper limit of normal (ULN) at Screening All known patients with the above and any patient with a personal or significant family history of thrombotic events (DVT, PE, arterial clots) as deemed by the principal investigator will be screened for the above disorders.
- Active invasive malignancy (Non-melanoma skin cancers and carcinoma in situ are not excluded).
- Known bone marrow disorders or abnormal bone marrow cytogenetics.
- Fertile males who are unwilling to use contraceptive techniques during and for the twelve months following treatment.
- Life expectancy severely limited by disease(s) other than hemophilia A.
- Patients with HIV, hepatitis B, hepatitis C (with an AST/ALT \> 3 times the upper limit of normal).
- Other active infectious disease that is a contraindicat ion for immunosuppressive therapy.
- Patients who have elective surgery scheduled during the study period.
Key Trial Info
Start Date :
April 29 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 1 2033
Estimated Enrollment :
5 Patients enrolled
Trial Details
Trial ID
NCT03818763
Start Date
April 29 2020
End Date
May 1 2033
Last Update
November 13 2025
Active Locations (1)
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1
Froedtert Hospital and the Medical College of Wisconsin
Milwaukee, Wisconsin, United States, 53226