Alector’s AL101 Receives FDA’s Fast Track Designation to Treat Frontotemporal Dementia

Shots:

• The US FDA has granted FT designation to Alector’s AL101 to treat patients with progranulin gene mutations causative of frontotemporal dementia (FTD-GRN), currently being evaluated in P-I study in healthy volunteers
• The FDA’s FT designation is designed to facilitate the development and expedite the review of therapies for serious conditions targeting unmet medical needs of patients
• AL101 is a mAb, designed to restore levels of progranulin in the CNS, currently in development for FTD-GRN, AD and PD and has received FDA’s ODD for FTD-GRN in July’2019

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