RecruitingPhase 1NCT05709288

Gene Therapy for Hemophilia B Patients Aged 12-18 Years Old

A Pilot Study Evaluating the Safety, Tolerability and Efficacy of Gene Therapy With BBM-H901 in Hemophilia B Patients Aged 12-18 Years Old


Sponsor

Institute of Hematology & Blood Diseases Hospital, China

Enrollment

9 participants

Start Date

Mar 23, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This is a Phase 1, open- label, non- randomized, uncontrolled, single dose pilot study to evaluate the safety, tolerability and efficacy of a single intravenous infusion of BBM-H901 in hemophilia B subjects with ≤2IU/dl residual FIX levels and aged 12-18 years old. BBM-H901 is an adeno-associated viral (AAV) vector designed to drive expression of the human factor IX (hFIX) transgene and raise circulating levels of endogenous FIX.


Eligibility

Sex: MALEMin Age: 12 YearsMax Age: 18 Years

Inclusion Criteria16

  • Subjects and statutory guardian must be able to understand the purpose and risks of the study and provide signed and dated informed consent;
  • Be male and 12≤ age <18 years of age, body wight ≥ 50kg;
  • Have hemophilia B with ≤2 IU/dL (≤2 %) endogenous FIX activity levels as documented by a certified clinical laboratory at the time of screening. If the screening result is >2% due to insufficient washout from FIX protein product, then the severity of hemophilia B may be confirmed by documented historical evidence from a certified clinical laboratory demonstrating ≤2% FIX coagulant activity (FIX:C) ;
  • Had had ≥75 prior exposure days (EDs) to any recombinant and/or plasma-derived FIX protein products based on historical data from the subject's record/history;
  • With ≤ 1:4 neutralizing antibodies and ≤1:200 binding antibodies against BBM-H901 capsid;
  • Subjects with bleeding episode and/ or FIX agents infusion events within 12 weeks prior to screening;
  • Have no prior history of hypersensitivity or anaphylaxis associated with any FIX or IV immunoglobulin administration;
  • Have no measurable FIX inhibitor as assessed by laboratory; or documented no prior history of FIX inhibitor (family history of inhibitors will not exclude the subject) and no clinical signs or symptoms of decreased response to FIX administration;
  • Have acceptable laboratory values:
  • Hemoglobin ≥11 g/dL ;
  • Platelets ≥100,000 cells/μL;
  • AST, ALT ≤1.5x upper limit of normal at the testing laboratory;
  • Bilirubin ≤1.5x ULN ;
  • glomerular filtration rate eGFR ≥ 60ml/min.
  • For those subjects with sexual maturity, subject and statutory guardian must know that subjects must agree to use reliable barrier contraception until 52 weeks;
  • with good compliance to the schedule of visit and fill in the subject diary.

Exclusion Criteria12

  • Hepatitis B surface antigen antibody (HBSAg-Ab) or HBV-DNA positive; hepatitis C antibody or HCV-RNA positive;
  • Currently on antiviral therapy for hepatitis B or C;
  • With coagulation disorders other than hemophilia B;
  • Had immunosuppressive therapy other than steroid and other suggested IST agents within 30 days prior to screening;
  • Had vaccine 30 days prior to screening or have scheduled vaccination plan during the study (up to 52 weeks);
  • Have significant underlying liver disease, as defined by a preexisting diagnosis of portal hypertension, splenomegaly, encephalopathy, etc; other liver conditions unsuitable to gene therapy judged by investigator;
  • Have surgery plan within 52 weeks after gene therapy;
  • Have history of chronic infection or high rish of infection that the Investigator considers to constitute an unacceptable risk;
  • Had participated in a previous gene therapy research trial within the last 52 weeks or in a clinical study with an investigational drug within the last 12 weeks;
  • Had any herb that may affect the liver function within 4 weeks prior to screening;
  • Have history of fatal bleeding episode, eg intracranial hemorrhage, etc;
  • Any concurrent clinically significant major disease or any other condition that, in the opinion of the Investigator, makes the subject unsuitable for participation in the study;

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Interventions

DRUGBBM-H901

Single dose intravenous infusion of BBM-H901, an adeno-associated viral (AAV) vector designed to drive expression of an hyper active human factor IX mutant(FIX Padua) transgene in liver. The dose of BBM-H901 is 5x10'12 vg/Kg.


Locations(1)

Institute of haematology and Blood diseases hospital

Tianjin, Tianjin Municipality, China

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NCT05709288


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