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Discovery Pharmacology for Alzheimer's Disease: Models, Mechanisms, Biomarkers

Alzheimer’s disease remains one of the most active and complex areas of CNS drug discovery—driving demand for preclinical models that offer mechanistic clarity, translational relevance, and adaptability across therapeutic modalities. As novel strategies continue to emerge, researchers are advancing in vitro and in vivo tools to better model disease biology, evaluate pharmacological response, and align with clinical biomarker frameworks.

Join Stefan Ebner-Benke, PhD, Director In Vivo, Scantox Neuro, for Discovery Pharmacology for Alzheimer's Disease: Models, Mechanisms, Biomarkers on September 23, 2025 | 15:00 CEST (9:00 AM EDT) followed by a Q&A session including panelists Irene Schilcher, PhD, Deputy Head of In Vitro Research & Roland Rabl, Scientific Account Director, Deputy Head of Study Coordination and expert in behavioral studies.

This session will explore how in vitro and in vivo models are used to investigate key mechanisms in Alzheimer’s disease—such as tau pathology, Aβ aggregation, neuroinflammation, and aging—and how these models are selected and adapted to support early discovery through candidate selection. The discussion will focus on practical considerations for study design, biomarker strategy, and aligning models with therapeutic modality and mechanism of action.

Key Learning Objectives

  • Review core and emerging Alzheimer’s models—considering key mechanisms like proteinopathy, neuroinflammation, and key risk factors such as aging—and how they support different stages of drug discovery.
  • Understand how preclinical models are used to evaluate translational biomarkers, target engagement, and disease modification.
  • Learn how to align model selection with program goals—from early screening to mechanism-of-action refinement.
  • Explore study design variables including modality, administration route, drug target, BBB strategy, and treatment timing.

Who Should Attend

  • Neuroscientists and discovery pharmacologists working in CNS drug development.
  • Translational researchers focused on Alzheimer’s disease.
  • Biotech and pharma teams developing novel modalities for neurodegeneration
  • Nonclinical consultants, CRO collaborators, and program strategists seeking fit-for-purpose models.

Meet The Presenter

Dr. Stefan Ebner-Benke brings extensive experience in the design, coordination, and execution of complex nonclinical studies supporting novel neuropharmacological discovery. As Director In Vivo  at Scantox Neuro, he partners with biotech and pharmaceutical clients to translate early-stage CNS research into actionable data through scientifically rigorous and operationally robust study programs. His multidisciplinary background spans academic research, strategic consulting, and nonclinical operations, with a proven track record of driving excellence in preclinical study delivery. He holds a PhD in Molecular Biology from the University of Vienna, an MSc in Molecular Microbiology from the University of Graz, and an Executive MBA from California Lutheran University.

Stefan Ebner-Benke, PhD, EMBA

Stefan Ebner-Benke, PhD, EMBA

Director In Vivo | Scantox Neuro

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Meet The Presenter

Dr. Matt Tate, PhD, is a recognized expert in genetic toxicology with over 20 years of experience at Gentronix, Part of Scantox Group. Initially focused on developing advanced screening assays, Matt transitioned into strategic leadership, shaping the company’s growth into a premier predictive toxicology CRO. With a deep operational understanding and extensive engagement with global regulatory bodies, he helps sponsors implement the most effective testing strategies to address mutagenicity concerns. Holding a BSc in Biochemistry from the University of Leeds and a PhD in Genetic Toxicology from the University of Manchester, Matt continues to bridge the gap between cutting-edge toxicology science and practical regulatory applications.

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Dr. Matt Tate, PhD

Managing Director, Gentronix, Part of Scantox Group