Study identifier:D2750C00002
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Open-Label Positron Emission Tomography Study with Selective Beta Amyloid Radioligand (18Fluor)AZD4694 to Assess the Effects of Varying Mass of AZD4694 on Radioligand Binding Parameters in Healthy Volunteers and Patients with Alzheimer's Disease
Maximum diagnostic mass of [18Fluor]AZD4694
Phase 1
Yes
-
Male
16
Interventional
50 Years - 85 Years
Allocation: Non-randomized
Endpoint Classification: Safety Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Basic Science
Verified 01 Dec 2012 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Part 1 Cohort 1 Patients with mild to moderate Alzheimer’s Disease | Other: [18Fluor]AZD4694 Low mass dose below 5ug. High mass dose around 40 and 50 ug. |
Experimental: Part 1 Cohort 2 Patients with mild to moderate Alzheimer's Disease. To run if Maximum Detective Mass is detected in cohort 1. | Other: [18Fluor]AZD4694 Low mass dose below 5ug. High mass dose around 20 ug. |
Experimental: Part 2 Healthy Volunteers | Other: [18Fluor]AZD4694 Low mass dose below 5ug. High mass dose will be the Maximum Detective Mass established in the previous panels. |