Lentiviral FVIII Gene Therapy

Official title

Lentiviral FVIII Gene Therapy for Hemophilia A

Overview

This study is a Phase I trial using an advanced lentiviral vector to deliver a functional gene for human clotting factor VIII into patients with hemophilia A, to evaluate the safety and efficacy of infusion of lentiviral gene modified autologous stem cells in patients.

Detailed description

Hemophilia A is a genetic bleeding disorder caused by the lack of ability to produce blood-clotting factor VIII (FVIII). Individuals with hemophilia A suffer repeated bleeding episodes, which can cause chronic joint disease and sometimes even death due to the inability for blood to clot efficiently. The current treatment is intravenous infusion of clotting factor concentrates, either prophylactically or in response to bleeding. The procedure is life time long and expensive while still cannot achieve a cure.Gene therapy is a novel technology that has been successfully demonstrated in a number of clinical studies for diseases such as cancer and genetic diseases. In this study, an advanced lentiviral vector system NHP/TYF will be used to deliver a functional FVIII gene to overcome human clotting FVIII gene defect in patients with hemophilia A. This study is a Phase I trial evaluating the safety and efficacy for infusion of gene modified autologous stem cells in patients with hemophilia A.

Interventions

• Biological YUVA-GT-F801
  Lentiviral factor VIII gene modified autologous hematopoeitic stem cells and mesenchymal stem cells

Primary outcome measures

• Number of participants experiencing drug-related adverse events [Time frame: a year]

Secondary outcome measures (1)

• Changes from baseline in circulating FVIII activity (IU/dL or % normal) [Time frame: a year]

Eligibility criteria

Inclusion criteria

• Able to provide informed consent and comply with requirements of the study.
• Males ≥2 years with confirmed diagnosis of hemophilia A (endogenous factor VIII ≤2 IU/dL or ≤2% of normal).
• A minimum average of 4 bleeding events per year requiring episodic treatment of factor VIII infusions or prophylactic factor VIII infusions.
• No measurable factor VIII inhibitor as assessed by the central laboratory and have no prior history of inhibitors to factor VIII protein.
• Agree to use reliable barrier contraception until 3 consecutive samples are negative for vector sequences.

Exclusion criteria

• Significant liver dysfunction as defined by abnormal alanine transaminase, bilirubin and alkaline phosphatase.
• History of inhibitor against factor VIII.
• Evidence of active hepatitis B or C and currently on antiviral therapy.
• Have serological evidence of HIV-1 or HIV-2 with CD4 counts ≤200/mm3 (subjects who are HIV+ and stable with CD4 count >200/mm3 and undetectable viral load are eligible to enroll).
• Any evidence of active infection or any immunosuppressive disorder.
• Participated in a gene transfer trial within the last 6 months or in a clinical trial with an investigational drug within the last 12 weeks.
• Unable or unwilling to comply with study assessments.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Non-randomized

Model

Single group

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Shenzhen Geno-immune Medical Institute — Shenzhen

Identifiers

NCT: NCT03217032 · GIMI-IRB-17007

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗