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An Open-Label, Expanded Access Protocol of LAM-002A in C9ORF72-Associated Frontotemporal Dementia (FTD)

Frontotemporal Dementia Clinical Trial

Official title:
An Open-Label, Expanded Access Protocol of LAM-002A (Apilimod Dimeyslate Capsules), Administered to a Single Subject With C9ORF72-Associated Frontotemporal Dementia (FTD)

Clinical Trial Summary

This is an open-label, single subject, expanded access protocol (EAP) of the LAM-002A investigational product administered orally at 125 mg BID for 52 weeks.

Clinical Trial Description

LAM-002A will be provided for expanded access for an individual patient under 21 CFR 312.310. It will be administered BID orally at a dose of 125 mg. Assessment of safety will include clinical observations and monitoring following administration. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05483322
Study type Expanded Access
Source AI Therapeutics, Inc.
Contact
Status No longer available
Phase
View Details
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