Shenzhen Children's Hospital
Shenzhen, Guangdong, 518083, China
Location status: Recruiting
NCT Number: NCT05745532
This is an open label study to evaluate the safety and efficacy of β-globin Restored Autologous Hematopoietic Stem Cells in ß-Thalassemia Major Patients
Interested in participating?
Request Info8 year–16 year
All sexes
Interventional
Early Phase 1
Shenzhen, Guangdong, 518083, China
Location status: Recruiting
We will recruit ß-thalassaemia major patients and collect their autologous hematopoietic stem cells, which will be modified with the LentiHBBT87Q system to restore β-globin expression. After conditioning, the autologous hematopoietic stem cells with restored β-globin will be reinfused to the patients and followed up for two years to collect data.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
β-globin-restored autologous hematopoietic stem cells modified with LentiHBBT87Q
Time frame: 0-100 days
The number and the percentage of adverse events related to transplantation in 100 days will be summarized according to NCI CTCAE 5.0
Time frame: 0-24 months
Number of patients alive through the whole trial will be record
Time frame: 0-24 months
Neutrophil count [ANC] >=500 /mm3 for 3 consecutive days and platelet count [PLT] >20,000/mm3 for7 consecutive days
Time frame: 0-24 months
The percentage of RCL should be negative in the 24 months after transplant
Time frame: 0-24 months
Evaluation of the percentage of participants without abnormal clonal proliferation and polyclonal engraftment . More than 1000 VIS retrieved from peripheral blood should be checked.
Time frame: 18-24 Months
The average insertion copy number (VCN) should be ≥0.1 in peripheral blood mononuclear cells
Time frame: 18-24 Months
Exogenous adult hemoglobin will be evaluated by globin chains and hemoglobin synthesis on peripheral blood by HPLC and the exogenous adult hemoglobin level is ≥2.0g/dL
Time frame: 18-24 Months
Compare the annualized number of pRBC transfusions before gene therapy with the Month 18 and Month 24 period after transplant, the percentage change will be recorded
Contact information is provided by the study sponsor or research team.
Shenzhen Hemogen
Industry
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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