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Lentiviral FIX Gene Therapy

Lentiviral FIX Gene Therapy for Hemophilia B

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03961243
Enrollment
10
Registered
2019-05-23
Start date
2027-06-01
Completion date
2028-12-31
Last updated
2026-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemophilia B

Keywords

Hemophilia B, factor IX, Gene therapylentiviral vector

Brief summary

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

Detailed description

Important Regulatory Notice: This trial record is only for global academic information registration on ClinicalTrials.gov. Neither the sponsor Beijing Meikang Jimian Biotechnology Co., Ltd. nor collaborator Shenzhen Geno-Immune Medical Institute has obtained NMPA clinical trial approval or clinical technology filing permission to carry out interventional cell therapy trials in mainland China. ClinicalTrials.gov registration alone does not represent legal approval by Chinese health and drug regulatory authorities. Hemophilia B is a genetic bleeding disorder caused by the lack of ability to produce blood-clotting factor IX (FIX). Individuals with hemophilia B 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 FIX gene to overcome human clotting FIX gene defect in patients with hemophilia B. This study is a Phase I trial evaluating the safety and efficacy for infusion of gene modified autologous stem cells in patients with hemophilia B.

Interventions

BIOLOGICALYUVA-GT-F901

Lentiviral factor IX gene modified autologous hematopoietic and mesenchymal stem cells

Sponsors

Shenzhen Geno-Immune Medical Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
2 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* 1\. Able to provide informed consent and comply with requirements of the study. 2. Males ≥2 years with confirmed diagnosis of hemophilia B (endogenous factor IX ≤2 IU/dL or ≤2% of normal). 3\. A minimum average of 4 bleeding events per year requiring episodic treatment of factor IX infusions or prophylactic factor IX infusions. 4\. No measurable factor IX inhibitor as assessed by the central laboratory and have no prior history of inhibitors to factor IX protein. 5\. Agree to use reliable barrier contraception until 3 consecutive samples are negative for vector sequences.

Exclusion criteria

* 1\. Significant liver dysfunction as defined by abnormal alanine transaminase, bilirubin and alkaline phosphatase. 2\. History of inhibitor against factor IX. 3. Evidence of active hepatitis B or C and currently on antiviral therapy. 4. 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). 5\. Any evidence of active infection or any immunosuppressive disorder. 6. 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. 7\. Unable or unwilling to comply with study assessments.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants experiencing drug-related adverse eventsa yearAs assessed by physical exam, vital signs, standard clinical labs, and Bethesda assay for FIX inhibitor

Secondary

MeasureTime frame
Changes from baseline in circulating FIX activity (IU/dL or % normal)a year

Countries

China

Contacts

CONTACTLung-Ji Chang, PhD
c@szgimi.org+86 0755-86573763
PRINCIPAL_INVESTIGATORLung-Ji Chang, PhD

Shenzhen Geno-Immune Medical Institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 27, 2026