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Terminated Phase 3 Interventional

Study of the Safety and Clinical Effects of 2 Doses of EVP-6124 in Subjects With Alzheimer's Disease Who Complete Study EVP-6124-024 or EVP-6124-025

ClinicalTrials.gov ID: NCT02004392

Public ClinicalTrials.gov record NCT02004392. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 5:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 26-Week Extension Study of the Safety and Clinical Effects of EVP-6124 in Subjects With Alzheimer's Disease Currently or Previously Receiving an Acetylcholinesterase Inhibitor Medication

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a 26-week, randomized extension of the Phase 3 double-blind placebo-controlled studies, EVP-6124-024 and EVP-6124-025. In this extension study, subjects who complete study EVP-6124-024 or EVP-6124-025 and fulfill all entry criteria will be randomized to receive EVP-6124 for an additional 26 weeks.

Study identification

NCT ID
NCT02004392
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
FORUM Pharmaceuticals Inc
Industry
Enrollment
348 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
55 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2014 (Type not available)
Primary completion
Aug 2017 (Estimated)
Completion
Aug 2017 (Estimated)
Last update posted
May 3, 2016

2014 – 2017

United States locations

U.S. sites
56
U.S. states
26
U.S. cities
56
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
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Not listed Creve Coeur Missouri — —
Not listed Princeton New Jersey — —
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Not listed Portland Oregon — —
Not listed Norristown Pennsylvania — —
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Not listed East Providence Rhode Island — —
Not listed San Antonio Texas — —
Not listed Salt Lake City Utah — —
Not listed Bennington Vermont — —
Not listed Charlottesville Virginia — —
Not listed Williamsburg Virginia — —
Not listed Richland Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02004392, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 3, 2016 · Synced Oct 20, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02004392 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →