Alzheimer's Disease Neuroimaging Initiative 2

NCT01231971 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1182

Last updated 2024-11-21

No results posted yet for this study

Summary

The purpose of this study is to build upon the information obtained in the original Alzheimer's Disease Neuroimaging Initiative (ADNI1) and ADNI-GO (Grand Opportunity; a study funded through an NIH grant under the American Recovery and Reinvestment Act), to examine how brain imaging technology can be used with other tests to measure the progression of mild cognitive impairment (MCI) and early Alzheimer's disease (AD). ADNI2 seeks to inform the neuroscience of AD. This information will aid in the early detection of AD, and in measuring the effectiveness of treatments in future clinical trials.

Conditions

  • Mild Cognitive Impairment (MCI)
  • Alzheimer's Disease (AD)
  • Significant Memory Concern (SMC)
  • Early Mild Cognitive Impairment (EMCI)
  • Late Mild Cognitive Impairment (LMCI)

Interventions

DRUG

Florbetapir

Participants will receive a single bolus intravenous injection of 10 mCi (370 MBq) (+/- 10%) florbetapir F18. At approximately 50-minutes post dose, scanning will begin. An approximately 20-minute image acquisition scan will be performed.

DRUG

Flortaucipir

Participants will receive a single bolus intravenous injection of 10 mCi (370 MBq) flortaucipir injection followed by a saline flush. At approximately 75-minutes post dose, scanning will begin. An approximately 30-minute image acquisition scan will be performed.

Sponsors & Collaborators

  • Northern California Institute of Research and Education

    collaborator OTHER
  • National Institute on Aging (NIA)

    collaborator NIH
  • Alzheimer's Therapeutic Research Institute

    collaborator OTHER
  • University of Southern California

    lead OTHER

Principal Investigators

  • Ronald Petersen, MD, PhD · Mayo Clinic

  • Michael W. Weiner, MD · University of California, San Francisco

  • Paul S. Aisen, MD · University of Southern California

Eligibility

Min Age
55 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-02-14
Primary Completion
2017-11-29
Completion
2017-11-29
FDA Drug
Yes

Countries

  • United States
  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01231971 on ClinicalTrials.gov