Clinical Trials Directory

Trials / Completed

CompletedNCT04135300

Gene Therapy for Chinese Hemophilia B

Gene Therapy for Chinese Hemophilia B With Adeno-associated Virus (AAV) Vector

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Institute of Hematology & Blood Diseases Hospital, China · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

GT2019001 is a Phase 1, open- label, non- randomized, uncontrolled, single dose pilot study to evaluate the safety, tolerability and kinetics of a single intravenous infusion of BBM-H901 in hemophilia B subjects with ≤2IU/dl residual FIX levels. 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.

Detailed description

GT2019001 is a Phase 1, open- label, non- randomized, uncontrolled, single dose pilot study to evaluate the safety, tolerability and kinetics of a single intravenous infusion of BBM-H901 in hemophilia B subjects with ≤2IU/dl residual FIX levels. Three subjects will be enrolled and administered with single infusion of BBM-H901, an AAV at one dose level of 5x1012 vg/Kg.Subjects will provide informed consent and then undergo screening assessments up to 4-8weeks prior administration of BBM-H901. All subjects will undergo 52(+- 2) weeks safety observation and will be encouraged to enroll in an extension study to evaluate long- term safety of BBM-H901 for a total 5 years.The first subject will be dosed at 5x1012 vg/Kg and undergo 2 months safety observation of which the data will undergo review by an independent safety committee. The dosing to the second subject will not be performed until acquiring the approve from independent safety committee.

Conditions

Interventions

TypeNameDescription
GENETICSingle dose intravenous injection of BBM-H901Single dose intravenous infusion of BBM-H901, an adeno-associated viral (AAV) vector designed to drive expression of the human factor IX (hFIX) transgene in liver. The dose of BBM-H901 will be 5x10'12 vg/Kg.

Timeline

Start date
2019-10-16
Primary completion
2022-01-07
Completion
2022-01-07
First posted
2019-10-22
Last updated
2025-02-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04135300. Inclusion in this directory is not an endorsement.