A Study of FVIII Gene Therapy for Hemophilia A

Prior treatment

• Currently on antiviral therapy for hepatitis B or C.
• Use of any other systematic immunosuppressant other than glucocorticoids within 30 days prior to enrollment.
• Patients with vaccination history within 30 days prior to screening.
• Patients with known planned major surgery schedule during the 52-week study period aren't eligible.
• Have participated in a previous gene therapy research trial before screening, or in a clinical study with an investigational drug within 5 half-life of the investigational product, whichever is longer.
• Have alcohol or drug dependence, or cannot stop drinking throughout the study. 10.Any concurrent clinically significant major disease or condition that the investigator deems unsuitable for participation in the study.

Other illness

• Being positive for hepatitis B surface antigen (HBsAg) or hepatitis B virus-DNA (HBV-DNA). Being positive for hepatitis C virus antibody (HCV-Ab) or hepatitis C virus RNA (HCV-RNA).
• Patients with coagulation disorders in addition to hemophilia A.

Lab values

• Have potential liver diseases, such as previous diagnosis of portal hypertension, splenomegaly, hepatic encephalopathy or liver fibrosis (fibrosis stage ≥ 3); nodules or cysts were found by B ultrasound, or elevated alpha-fetoprotein was detected by laboratory tests. Subjects who are not eligible for the study if the abnormalities are clinically significant by researchers.

• Subjects are fully aware of the purpose, nature, methods and possible adverse reactions of the trial and voluntarily sign informed consent.
• Males ≥ 18 years of age.
• Have hemophilia A with ≤2 IU/dL (≤2 %) endogenous FVIII activity levels.
• Have had ≥150 prior exposure days (EDs) to any recombinant and/or plasma-derived FVIII protein products.
• Have had bleeding events and/or infusions with FVIII protein products (including recombination and plasma source) during the last 12 weeks documented in the subjects' medical records.
• Have no prior history of hypersensitivity or anaphylaxis associated with any FVIII or IV immunoglobulin administration.
• Have no FVIII inhibitor. (eg \<0.6BU/ml Bethesda Units; or the patient's FVIII inhibitor titer was detected \<0.6BU/ml in 2 consecutive times within 1-4 weeks using Bethesda method or Nijmegen method), or no prior medical history of FVIII inhibitor after 150 EDs of FVIII products; no clinical signs or symptoms of decreased response to FVIII products infusion.
• Agree to use a reliable barrier contraception method from the beginning of signing the informed consent to 52 weeks after BBM002 infusion.
• Compliance is good, patients and their families have the will of 'gene therapy' clinical trials.