Immix Biopharma Investor Presentation Deck slide image

Immix Biopharma Investor Presentation Deck

Adverse Event Profile - NXC-201 Adverse Events Cytokine Release Syndrome (CRS) Day of median onset (min-max) Days of median duration (min-max) Immune cell associated Neurotoxicity (ICANS) Day of median onset (min-max) Day of median duration (min-max) Toxicity Management | Tocilizumab | Dexamethasone NXC-201 150x10 CAR+T cells n=6 Grade 3 0 (0%) 0 (0%) of n=6 1 (17%) 0 (0%) NXC-201 450x10 CAR+T cells n=7 Grade 3 0 (0%) 0 (0%) of n=7 4 (57%) 0 (0%) Grade 1-2 41 (82%) 1 2 (4%) NXC-201 800x10 CAR+T cells n=50 of n=50 40/48 (83%) 8/48 (17%) ●●● IMMIX S BIOPHARMA Grade 3 7 (14%) 2 0 (0%) Note. No Grade 4 CRS with NXC-201. Source: Development and manufacturing of novel locally produced anti-BCMA CART cells for the treatment of relapsed/refractory multiple myeloma: phase I clinical results. Haematologica. 2022 Oct 6. doi: 10.3324/haematol.2022.281628. Epub ahead of print. PMID: 36200421, Point-of-care CART manufacture and delivery: Expanding access to CART therapy via local institutions, Hadassah Medical Center experience. Poster Presentation, European Society for Blood and Marrow Transplantation and European Hematology Association 5th European CAR T-cell Meeting. 2023 Feb 9-11, Nexcella, Inc. E. Lebel et al. Efficacy and Safety of a Locally Produced Novel Anti-BCMA Chimeric Antigen Receptor T-Cell (CART) (HBI0101) for the Treatment of Relapsed and Refractory Multiple Myeloma, International Myeloma Society 20th Annual Meeting. 2023. 39
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