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Clinical Trials associated with Gene-modified autologous stem cell therapy (Shenzhen Geno-Immune Medical Institute) / Not yet recruitingEarly Phase 1IIT Clinical study for the efficacy and safety of gene-corrected autologous hematopoietic stem cell transplantation in the treatment of severe β-thalassemia
Start Date01 Apr 2020 |
Sponsor / Collaborator- |
/ Not yet recruitingEarly Phase 1IIT Clinical study for the effectiveness and safety of gene-corrected autologous hematopoietic stem cell transplantation in the treatment of hemophilia B
Start Date01 Apr 2020 |
Sponsor / Collaborator- |
/ Unknown statusNot ApplicableIIT Gene Transfer for Fanconi Anemia Using a Self-inactivating Lentiviral Vector
This is a Phase I/II clinical trial of gene therapy for treating Fanconi anemia using a self-inactivating lentiviral vector to functionally correct the defective gene. The objectives are to evaluate the safety and efficacy of the gene transfer clinical protocol.
100 Clinical Results associated with Gene-modified autologous stem cell therapy (Shenzhen Geno-Immune Medical Institute)
100 Translational Medicine associated with Gene-modified autologous stem cell therapy (Shenzhen Geno-Immune Medical Institute)
100 Patents (Medical) associated with Gene-modified autologous stem cell therapy (Shenzhen Geno-Immune Medical Institute)
100 Deals associated with Gene-modified autologous stem cell therapy (Shenzhen Geno-Immune Medical Institute)