LEXEO Therapeutics Receives the US FDA’s Fast Track Designation for LX1001 to Treat APOE4 Associated Alzheimer Disease

April 21, 2021 Auto Bot Alzheimer Disease, Fast Track Designation, FDA, receives, regulatory, Treatment 0

Shots:

  • The US FDA has granted FT Designation to LX1001 for the treatment of APOE4 associated AD. The designation evaluates to facilitate the development and expedite the review of drug
  • The company has initiated P-I trial to assess the safety and toxicity of LX1001 as a potential one-time treatment for early-stage AD patients with mild cognitive impairment who are APOE4 homozygous
  • The study will establish a maximum tolerable dose and is expected to complete dosing of 15 patients in 2021 while the initial P-I clinical data are expected in the H2’21

Click here to­ read full press release/ article | Ref: Globe Newswire | Image: Yahoo Finance

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