Low phosphate levels linked with CAR T neurological toxicity October 20, 2022 -- Patients with hypophosphatemia had higher incidences and more severe neurological side effects on chimeric antigen receptor (CAR) T-cell therapy than those with normal blood phosphate levels, according to a study published October 19 in the journal Cancer Immunology Research.Read More
Platform enables precise, efficient delivery of genetic medicines in vivo October 17, 2022 -- Biotech company Homology Medicines is leveraging 15 human hematopoietic stem cell-derived adeno-associated virus vectors to precisely and efficiently deliver genetic medicines in vivo via gene therapy or nuclease-free gene editing modality. CEO Albert Seymour spoke with Science Advisory Board about their platform.Read More
Manufacturing remains big challenge for cell and gene therapy industry October 17, 2022 -- Science Advisory Board spoke with Eric Blair, chief commercial officer for Andelyn Biosciences, at last week’s 2022 Cell & Gene Meeting on the Mesa about the challenges of manufacturing to meet growing demand in the cell and gene therapy industry.Read More
Gene editing advances continue a pace, but progress is still early: panel October 17, 2022 -- With the first-ever approval of a CRISPR gene editing therapy expected in 2023, companies at last week’s Cell & Gene Meeting on the Mesa say they are looking forward to other near- and longer-term breakthrough technologies on the horizon.Read More
FDA biologics chief outlines ways to remove barriers to cell and gene therapies October 13, 2022 -- At this year's Meeting on the Mesa, the U.S. Food and Drug Administration’s top biologics regulator said the use of a “cookbook” for developing cell and gene therapy products and global regulatory convergence could help to facilitate their development and take them to the next level.Read More
Gene therapy one step closer to delivery across blood-brain barrier: study October 11, 2022 -- Brigham and Women’s Hospital researchers say the rational design of adeno-associated viruses has generated gene therapy delivery vectors that are better at crossing the blood-brain barrier to treat diseases of the central nervous system.Read More