2
Clinical Trials associated with TYF-IL-2Rg gene-modified autologous stem cells(Shenzhen Geno-Immune Medical Institute)Gene Therapy for X-linked Severe Combined Immunodeficiency (SCID-X1) Via Direct Intravenous Injection of Lentiviral Vector (Ivlv-X1)
This is a Phase I/II gene therapy trial treating X-linked severe combined immunodeficiency (SCID-X1) using a self-inactivating lentiviral vector (ivlv-X1) to functionally correct the genetic defect. The primary objectives are to evaluate the safety and efficacy of the direct intravenous lentiviral gene transfer protocol.
/ Unknown statusNot ApplicableIIT Lentiviral Gene Therapy for Chronic Granulomatous Disease (CGD)
This is a Phase I/II clinical trial of gene therapy for treating Chronic Granulomatous Disease using a high-safety, high-efficiency, self-inactivating lentiviral vector TYF to functionally correct the defective gene. The objectives are to evaluate the safety and efficacy of the TYF-CGD gene transfer clinical protocol.
100 Clinical Results associated with TYF-IL-2Rg gene-modified autologous stem cells(Shenzhen Geno-Immune Medical Institute)
100 Translational Medicine associated with TYF-IL-2Rg gene-modified autologous stem cells(Shenzhen Geno-Immune Medical Institute)
100 Patents (Medical) associated with TYF-IL-2Rg gene-modified autologous stem cells(Shenzhen Geno-Immune Medical Institute)
100 Deals associated with TYF-IL-2Rg gene-modified autologous stem cells(Shenzhen Geno-Immune Medical Institute)