FDA grants breakthrough designation to frontotemporal dementia treatment

Key takeaways: 

  • Latozinemab is an investigational human monoclonal antibody.
  • The drug is currently being examined in a phase 3 clinical trial.

The FDA has granted breakthrough therapy designation to latozinemab, an investigational therapeutic designed to block sortilin and elevate progranulin to treat frontotemporal dementia with a progranulin gene mutation.

According to a press release from Alector Inc., the breakthrough designation was approved based on data from the phase 2 INFRONT-2 clinical trial of latozinemab in patients with the condition.

https://www.healio.com/news/neurology/20240208/fda-grants-breakthrough-designation-to-frontotemporal-dementia-treatment

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