Evaluation of the Safety and Efficacy of KL003 Gene Therapy in Patients With Transfusion-dependent β-thalassemia With No Conditioning Regimen

Status: Recruiting
Location: See location...
Intervention Type: Genetic
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a non-randomized, open-label, single-dose study. The aim of this study is to evaluate the safety and efficacy of the treatment with lentiviral vector encoding βA-T87Q-globin gene transduced autologous hematopoietic stem cells transfusion in subjects with transfusion-dependent β-thalassemia.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 35
Healthy Volunteers: f
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• Male or female age between 3-35 years

• Diagnosis of transfusion-dependent β-thalassemia and a history of at least 100 mL/kg/year of pRBCs or ≥8 transfusions of pRBCs per year for the prior 2 years

• Documented baseline, or pretransfusion, Hb level≤7 g/dL

• Karnofsky performance status ≥70 for subjects≥16 years of age; Lansky performance status of ≥70 for subjects\<16 years of age

• Eligible to undergo auto-HSCT

• Willing and able to follow the research procedures and conditions, with good compliance

• Willing to receive at least the 2 years follow-up and maintain detailed medical records, including transfusion history

• Subject and/or legal guardians voluntarily participated in this clinical trial and signed the informed consent form, and can complete all follow-ups in accordance with the protocol requirements

Locations
Other Locations
China
Institute of Hematology & Blood Diseases Hospital
RECRUITING
Tianjin
Contact Information
Primary
Jun Shi, PhD
shijun@ihcams.ac.cn
13752253515
Backup
Zhen Gao, MD
gaozhen@ihcams.ac.cn
Time Frame
Start Date: 2024-01-04
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 3
Treatments
Experimental: KL003 cell injection Drug Product
Traditional myeloablative conditioning regimen consists of Busulfan, which may increase the risk of irreversible pulmonary fibrosis, VOD, and infertility due to potential serious toxicity. In this study, we intend to use genetic hematopoietic stem cells (lentivirus transduction) transfusion with no conditioning regimen, which could avoid toxicity due to chemotherapy drugs.
Sponsors
Leads: Institute of Hematology & Blood Diseases Hospital, China
Collaborators: Kanglin Biotech

This content was sourced from clinicaltrials.gov

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