Clinical Trials Directory

Trials / Terminated

TerminatedNCT01953601

Efficacy and Safety Trial of Verubecestat (MK-8931) in Participants With Prodromal Alzheimer's Disease (MK-8931-019)

A Phase III, Randomized, Placebo-Controlled, Parallel-Group, Double-Blind Clinical Trial to Study the Efficacy and Safety of MK-8931 (SCH 900931) in Subjects With Amnestic Mild Cognitive Impairment Due to Alzheimer's Disease (Prodromal AD)

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
1,454 (actual)
Sponsor
Merck Sharp & Dohme LLC · Industry
Sex
All
Age
50 Years – 85 Years
Healthy volunteers
Not accepted

Summary

This study consists of two parts, Part 1 and Part 2. Part 1 assesses the efficacy and safety of verubecestat (MK-8931) compared with placebo administered for 104 weeks in the treatment of amnestic mild cognitive impairment (aMCI) due to Alzheimer's Disease (AD), also known as prodromal AD. Participants are randomized to receive placebo, or 12 mg or 40 mg verubecestat, once daily. The primary study hypothesis for Part 1 is that ≥1 verubecestat dose is superior to placebo with respect to the change from baseline in the Clinical Dementia Rating scale-Sum of Boxes (CDR-SB) score at 104 weeks. Participants completing Part 1 may choose to participate in Part 2, which is a long term double-blind extension to assess efficacy and safety of verubecestat administered for up to an additional 260 weeks. In Part 2, all participants receive either 12 mg or 40 mg verubecestat, once daily.

Detailed description

As a result of protocol amendment, Study Part 2 will contain a Positron Emission Tomography (PET) imaging substudy to assess regional neurofibrillary tangle (NFT) expression.

Conditions

Interventions

TypeNameDescription
DRUGVerubecestat 12 mg (Parts 1 and 2)Verubecestat 12 mg oral tablet, given once daily.
DRUGVerubecestat 40 mg (Parts 1 and 2)Verubecestat 40 mg oral tablet, given once daily. Verubecestat 40 mg given to participants in Arm C continuing to study Part 2.
OTHERPlacebo (Part 1)Placebo matching verubecestat, given once daily as an oral tablet.

Timeline

Start date
2013-11-05
Primary completion
2018-04-17
Completion
2018-04-17
First posted
2013-10-01
Last updated
2019-05-17
Results posted
2019-05-17

Source: ClinicalTrials.gov record NCT01953601. Inclusion in this directory is not an endorsement.

Efficacy and Safety Trial of Verubecestat (MK-8931) in Participants With Prodromal Alzheimer's Disease (MK-8931-019) (NCT01953601) · Clinical Trials Directory