About this trial
Thalassemia is a group of recessively inherited hemoglobin disorders characterized by reduced or no production of hemoglobin and chronic anemia of varying severity. Severe β-thalassemia is transfusion-dependent thalassemia (TDT) and requires life-long transfusion, iron overload is a common complication of TDT. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a curative option currently available for TDT, but it carries significant acute and long-term risks. In this study, the autologous HSCT-based gene therapy (referred to as "gene therapy for thalassemia, " by using HGI-001) is based on the principle that the autologous haemopoietic stem cells (HSCs) collected from the patient him/herself are transduced outside human body, which will restore the function of RBCs, so as to achieve the effect of treating or even curing thalassemia. Currently data suggests that gene therapy for TDT patients has shown remarkable therapeutic effects, avoiding immune rejection, and is widely accepted by the medical community, positioning it as a highly promising treatment approach. To date, the efficacy and safety of HGI-001 have been evaluated through both in vitro and in vivo studies. In an early-phase clinical study of HGI-001 conducted in China, five patients achieved transfusion-independent post-treatment. Among them, four have maintained this state for over two years, with the longest duration reaching 3.5 years. The study noted no severe adverse events. The long-term safety and efficacy of HGI-001 continue to be under active surveillance.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Subjects between 12 and 45 years of age at the time of consent and are able to provide written informed consent.
Diagnosis of TDT, also known as β-thalassemia major, without genotype restriction, and a valid test report can be provided.
A history of at least 100 mL/kg/year of pRBCs transfusion or ≥ 8 transfusions of pRBCs per year for previous 2 years.
Sufficient blood transfusion for at least 3 months before screening (transfusion records can be provided), and Hb is maintained ≥9.0 g/dL before each transfusion.
Disqualifiers
Uncorrected bleeding disorder;
Uncontrolled epilepsy or mental disorders;
Received hydroxyurea, ruxolitinib, decitabine, or cytarabine within 3 months prior to enrollment;
Usage of psychoactive substance, drug, or alcohol abuse within six months prior to screening.
Trial design
Single group
Treatments tested in this trial
HGI-001 Injection
DrugHGI-001 Injection is the transduction of autologous CD34+ HSPCs by the lentiviral vector, named LentiHBBT87Q
Treatment groups
Trial outcomes
Primary outcomes
achieve transfusion independence (TI)for at least ≥12 months after HGI-001 Injection infusion
Subjects achieve transfusion independence (TI), which is defined as a weighted average Hb ≥9 g/dL without any pRBC transfusions at any time for a continuous period of ≥12 months during the study after HGI-001 Injection infusion
Locations
Sponsors and contacts
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