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AC Immune Presents First In vivo Images of Brain TDP-43 Pathology from Phase 1 Trial of PET tracer ACI-19626, at AD/PDTM 2026

AC Immune Presents First In vivo Images of Brain TDP-43 Pathology from Phase 1 Trial of PET tracer ACI-19626, at AD/PDTM 2026 Initial data indicates

articleAc Immune SaMarch 19, 20264/company/ac-immune-ltd/news/ac-immune-presents-first-in-vivo-images-of-brain-tdp-43-pathology-from-phase-1-trial-of-pet-tracer-aci-19626-at-adpdtm-2026
AC Immune Presents First In vivo Images of Brain TDP-43 Pathology from Phase 1 Trial of PET tracer ACI-19626, at AD/PDTM 2026

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[{"type":"text","content":"AC Immune Presents First In vivo Images of Brain TDP-43 Pathology from Phase 1 Trial of PET tracer ACI-19626, at AD/PDTM 2026 Initial data indicates significantly higher tracer uptake in patients with genetically defined FTDGood safety and tolerability and suitable PK profile for human brain imagingPotentially enables precision medicine across multiple neurodegenerative diseases Lausanne, Switzerland, March 19, 2026 -- AC Immune SA (NASDAQ: ACIU), a clinical-stage biopharmaceutical company pioneering precision therapeutics for neurodegenerative diseases, today announced the presentation of Phase 1 data including the first in vivo images of TDP-43 pathology in the human brain, detected using its first-in-class positron emission tomography (PET) tracer ACI-19626, at the International Conference on Alzheimer’s and Parkinson’s Disease (AD/PD™ 2026). Initial data from the Phase 1 trial support ACI-19626’s potential to detect pathological TDP-43 in the brains of patients with TDP-43 proteinopathies, enabling a precision medicine approach to multiple neurodegenerative diseases. Specifically, PET scans with ACI-19626 showed that tracer uptake was significantly higher in key regions of the brain in patients with frontotemporal dementia (FTD) due to mutated C9orf72 than in the brains of healthy subjects. As presented, regions with higher tracer uptake included subcortical and cortical regions of the brain where TDP-43 pathology is expected based on post-mortem neuropathology studies. ACI-19626 showed good safety and tolerability, a dosimetry profile within accepted limits, and rapid brain uptake and washout, indicating a pharmacokinetic (PK) profile suitable for human brain imaging and potentially pharmacodynamic analysis of therapeutics targeting TDP-43 pathology. Dr. Andrea Pfeifer, CEO of AC Immune SA, commented: “These first-in-human data presented at AD/PD™ are very encouraging and indicate that ACI-19626 could have an important role in early diagnosis of multiple neurogenerative diseases, with a clear path to precision medicine. This underlines the potential of the AC Immune pipeline, based on our SupraAntigen® and Morphomer® technology platforms, for precision prevention of multiple conditions, encompassing diagnostics, active immunotherapies and small molecules for intracellular targeting. We are looking forward to final data from...

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