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Clinical Trial Summary

This study will assess the effects of administration of VX-745 for 12 weeks on amyloid plaque burden in Alzheimer's disease (AD). Subjects who meet entry criteria will undergo 11C-PiB (Carbon-11-labeled Pittsburgh Compound B) positron emission tomography (PET) at baseline and after 45 days of dosing with VX-745. Cognitive testing will also be conducted at baseline and day 45.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02423122
Study type Interventional
Source EIP Pharma, LLC
Contact
Status Completed
Phase Phase 2
Start date April 2015
Completion date September 2016

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