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
1 Location
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