Investor presentation
Logotype for AC Immune SA

AC Immune (ACIU) Investor presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for AC Immune SA

Investor presentation summary

23 Sep, 2026

Strategic focus and differentiation

  • Pipeline targets neurodegenerative diseases with active immunotherapies and small molecules, emphasizing precision in toxic protein targeting.

  • Technology platforms validated by multiple clinical candidates and partnerships with major pharma companies.

  • Over CHF 4.3 billion in potential milestone payments from strategic partnerships.

  • Cash reserves of CHF 75.4 million, funding operations into Q4 2027.

  • Approximately 120 employees, based in Lausanne, Switzerland, and listed on NASDAQ.

Pipeline and clinical development

  • Active immunotherapies include ACI-24 (anti-Abeta), ACI-35 (anti-pTau), and ACI-7104 (anti-a-syn), with multiple candidates in Phase 1–3 trials.

  • Intracellular targeting programs focus on Tau, a-synuclein, and NLRP3 inflammasome, with both therapeutic and diagnostic applications.

  • Key 2026 milestones: Phase 2 trial results for ACI-24 in Alzheimer's, Phase 2 VacSYn trial in Parkinson's, and Phase 1/1b results for NLRP3 inhibitor.

  • Biomarker-driven, adaptive study designs enable dose optimization and early regulatory engagement.

  • FDA Fast Track designations for several programs, accelerating development timelines.

Clinical results and safety

  • ACI-7104 in early Parkinson's shows strong immunogenicity, 100% responder rate, and favorable safety profile with no significant adverse events.

  • ACI-24 Phase 1b/2 study in Alzheimer's and Down syndrome uses biomarker endpoints and adaptive dosing.

  • ACI-35 is the only active immunotherapy in a prevention study for pre-symptomatic Alzheimer's, with Phase 2 trial underway.

  • NLRP3 inhibitor ACI-19764 demonstrated safety, CSF exposure, and dose-dependent IL-1β inhibition in Phase 1.

  • Morphomer small molecules show in vivo efficacy in reducing Tau pathology and neuron loss in preclinical models.

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