Biomarker Qualification for Risk of Mild Cognitive Impairment (MCI) Due to Alzheimer's Disease (AD) and Safety and Efficacy Evaluation of Pioglitazone in Delaying Its Onset (TOMMORROW)
A Double Blind, Randomized, Placebo Controlled, Parallel Group Study to Simultaneously Qualify a Biomarker Algorithm for Prognosis of Risk of Developing Mild Cognitive Impairment Due to Alzheimer's Disease (MCI Due to AD) and to Test the Safety and Efficacy of Pioglitazone (AD-4833 SR 0.8 mg QD) to Delay the Onset of MCI Due to AD in Cognitively Normal Subjects
Sponsor: Takeda
Terminated
Lack of efficacy of the drug; no safety concern
Other terminated trials from Takeda
Other Mild Cognitive Impairment Due to Alzheimer's Disease trials with similar outcome
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A PHASE3 clinical study on Mild Cognitive Impairment Due to Alzheimer's Disease, this trial is terminated or withdrawn. The trial is conducted by Takeda and has accumulated 10 data snapshots since 2013. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
10 versions recorded-
Sep 2025 — Present [monthly]
Terminated PHASE3
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Sep 2024 — Sep 2025 [monthly]
Terminated PHASE3
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Jul 2024 — Sep 2024 [monthly]
Terminated PHASE3
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Jan 2021 — Jul 2024 [monthly]
Terminated PHASE3
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Oct 2019 — Jan 2021 [monthly]
Terminated PHASE3
▶ Show 5 earlier versions
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Sep 2019 — Oct 2019 [monthly]
Terminated PHASE3
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Sep 2018 — Sep 2019 [monthly]
Terminated PHASE3
Status: Active Not Recruiting → Terminated
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Jun 2018 — Sep 2018 [monthly]
Active Not Recruiting PHASE3
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Feb 2017 — Jun 2018 [monthly]
Active Not Recruiting PHASE3
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Jan 2017 — Feb 2017 [monthly]
Active Not Recruiting PHASE3
First recorded
Aug 2013
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Takeda
- Zinfandel Pharmaceuticals Inc.
For direct contact, visit the study record on ClinicalTrials.gov .