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Expert Interview

Slingshot members are talking to an expert! The topic is:

Discussing Novo Nordisk's Semaglutide prior to the topline data readout of the ongoing Phase 3 evoke and evoke+ trials for early-stage Alzheimer’s disease

Ticker(s): NVO

Who's the expert?

Institution: University of Kansas

  • Director of NIH-funded University of Kansas Alzheimer's Disease Center.
  • Currently manages 300 patients with Alzheimer's disease.
  • Research is focused on brain energy metabolism, the role brain energy metabolism plays in Alzheimer's Disease, and how to manipulate brain energy metabolism.

Interview Questions
Q1.

How important are the biomarker components of these trials, such as neuroinflammatory markers, amyloid/tau measures, and CSF analyses, in interpreting whether semaglutide is having a disease-modifying effect?

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Q2.

If semaglutide ultimately shows a significant benefit, how do you envision it fitting into the current AD treatment landscape alongside monoclonal antibodies like lecanemab and donanemab?

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Q3.

Are there specific safety or tolerability considerations unique to older adults with early AD that you believe will influence clinical uptake if semaglutide becomes an approved therapy?

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Q4.

From a trial-design perspective, what stands out to you about evoke/evoke+ (e.g., long treatment duration, oral formulation, amyloid-confirmed population), and what factors will most strongly determine whether the results are clinically meaningful?

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