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Terminated Phase 3 Interventional Results available

AD-4833/TOMM40_303 Extension Study of the Safety and Efficacy of Pioglitazone to Slow Cognitive Decline in Participants With Mild Cognitive Impairment Due to Alzheimer Disease

ClinicalTrials.gov ID: NCT02284906

Public ClinicalTrials.gov record NCT02284906. 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 Jun 26, 2026, 8:40 AM 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 Blinded Long-term Extension Study to Evaluate the Safety and Efficacy of Pioglitazone (AD-4833 Sustained Release 0.8 mg Daily) to Slow the Progression of Cognitive Decline in Subjects Who Have Completed the AD-4833/TOMM40_301 Study With Diagnosis of Mild Cognitive Impairment Due to Alzheimer Disease

Study identification

NCT ID
NCT02284906
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
40 participants

Conditions and interventions

Interventions

  • Pioglitazone Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
65 Years and older
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
Feb 11, 2015
Primary completion
Jan 30, 2018
Completion
May 7, 2018
Last update posted
Jul 1, 2019

2015 – 2018

United States locations

U.S. sites
28
U.S. states
16
U.S. cities
28
Facility City State ZIP Site status
Not listed Phoenix Arizona 85006
Not listed Sun City Arizona 85351
Not listed San Diego California 92103
Not listed Delray Beach Florida 33445
Not listed Fort Myers Florida 33912
Not listed Lake Worth Florida 33449
Not listed Melbourne Florida 32940
Not listed Merritt Island Florida 32952
Not listed Port Orange Florida 32127
Not listed St. Petersburg Florida 33709
Not listed Weston Florida 33331
Not listed Atlanta Georgia 30329
Not listed Decatur Georgia 30033
Not listed Chicago Illinois 60640
Not listed Elk Grove Illinois 60007
Not listed Elk Grove Village Illinois 60007
Not listed Iowa City Iowa 52242
Not listed St Louis Missouri 63141
Not listed Las Vegas Nevada 89106
Not listed Marlton New Jersey 08053
Not listed New York New York 10019
Not listed Concord North Carolina 28025
Not listed Durham North Carolina 27705
Not listed Akron Ohio 44320
Not listed Charleston South Carolina 29401
Not listed Houston Texas 77030
Not listed Salt Lake City Utah 84107
Not listed Middleton Wisconsin 53562

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 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02284906, 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 Jul 1, 2019 · Synced Jun 26, 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 protocol, eligibility criteria, and contact information for NCT02284906 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →