Session Details

Speakers, titles, times, and locations of ASGCT presentations

Detailed Program

Cell Therapy and Cell-Based Gene Therapy Trials

Session Details

Co-Chair

Co-Chair

240: FVIII Expression through Autologous CD34+ Hematopoietic Stem Cells Transduced with a Lentiviral Vector with a Novel F8 Transgene for Gene Therapy of Hemophilia A - A First-in-Human Clinical Trial

241: Investigation of mRNA Cell Therapy as a Treatment for Autoimmune Disease in Patients with Myastenia Gravis

242: Safety, Tolerability, and Clinical Assessment of Bemdaneprocel for Parkinson’s Disease: Results up to 18 Months from a Phase 1 Study

243: Eighteen-Year Follow-Up of GD2 Chimeric Antigen Receptor-Cytotoxic T Lymphocyte Therapy in Patients with Neuroblastoma

244: Efficacy and Safety of BRL-101, CRISPR-Cas9-Mediated Gene Editing of The BCL11A Enhancer in Transfusion-Dependent β-Thalassemia

245: Lentiviral-Mediated Gene Therapy (RP-L102) for Fanconi Anemia [Group A] is Associated with Polyclonal Integration Patterns in the Absence of Conditioning

246: Autologous Ex-Vivo Lentiviral Gene Therapy for Pediatric Patients with Severe Leukocyte Adhesion Deficiency-I Provides Sustained Efficacy with a Favorable Safety Profile

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