Assess 123-I IMPY and SPECT Imaging as a Tool to Detect β-Amyloid in the Brain

Completed · Phase 1

Conditions studied: Alzheimer Disease

In brief

This research is designed to obtain efficacy and safety information for 123-I IMPY as an imaging biomarker for Alzheimer's disease (AD). The distribution of this agent will be measured by obtaining single photon emission computed tomography (SPECT) images of the brain serially over time to determine the relative localization of the radiopharmaceutical in regions of the cortex relative to background regions and develop an optimal technique of radiotracer administration (bolus or bolus with constant infusion). The researchers will then evaluate the utility of 123-I IMPY and SPECT in AD patients as an early diagnostic tool and subsequently serial evaluations of AD patients will be performed to determine if this technique may be useful as a tool for evaluation of progressive brain β-amyloid deposition in AD.

Key facts

Study ID

NCT00287248

Run by

Institute for Neurodegenerative Disorders

People needed

38

Starts

2006-02-01

Expected to finish

2008-03-01

Last updated by the study team

2014-03-07

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• The participant is 50 years or older.
• Written informed consent is obtained.
• Participants have a clinical diagnosis of Alzheimer's disease based on National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer's Disease and Related Disorders Association (NINCDS/ADRA) criteria.
• Mini-Mental Status Exam score > 16 and < 25.
• Patients have a diagnosis of probable AD for < 3 years prior to screening.

You may not qualify if…

• The subject has signs or symptoms of another neurodegenerative disease including Parkinson's disease, diffuse Lewy body dementia, or history of significant cerebrovascular disease.
• Subjects with an iodine allergy.
• The subject has a clinically significant clinical laboratory value and/or medical or psychiatric illness.
• The subject has any disorder that may interfere with drug absorption distribution, metabolism, or excretion (including gastrointestinal surgery).
• The subject has evidence of clinically significant thyroid disease, gastrointestinal, cardiovascular, hepatic, renal, hematologic, neoplastic, endocrine, neurologic, immunodeficiency, pulmonary, or other medical or psychiatric disorder.
• The subject has received an investigational drug within 60 days before the screening visit.
• Pregnancy

Where it is running

• Institute for Neurodegenerative Disorders — New Haven, Connecticut, United States

Full record on ClinicalTrials.gov

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