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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

Trial Profile

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

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 17 Sep 2019

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At a glance

  • Drugs Pioglitazone (Primary)
  • Indications Alzheimer's disease; Mild cognitive impairment
  • Focus Registrational; Therapeutic Use
  • Acronyms TOMMORROW
  • Sponsors Takeda
  • Most Recent Events

    • 10 Feb 2019 This study has been completed in United Kingdom.
    • 31 Aug 2018 Biomarkers information updated
    • 25 Jan 2018 According to a Takeda media release, results from the study will be presented at a future scientific meeting.
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