A first in human phase 1 study in healthy volunteers and heterozygous carriers of a loss-of-function Granulin mutation causative of frontotemporal dementia to assess AL001 safety tolerability pharmacokinetics and pharmacodynamics

Recruiting
99 years or below
All
Phase 1
12 participants needed

Brief description of study

Please see section 1 of protocol

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: TBD
  • Age: 99 years or below
  • Gender: All
Updated on 19 Feb 2024. Study ID: 831627

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