Trials / Completed
CompletedNCT01028053
Assess the Prognostic Usefulness of Flutemetamol (18F) Injection for Identifying Subjects With Amnestic Mild Cognitive Impairment Who Will Convert to Clinically Probable Alzheimer's Disease
A Principal Open-label Study to Assess the Prognostic Usefulness of Flutemetamol (18F) Injection for Identifying Subjects With Amnestic Mild Cognitive Impairment Who Will Convert to Clinically Probable Alzheimer's Disease
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 365 (actual)
- Sponsor
- GE Healthcare · Industry
- Sex
- All
- Age
- 60 Years
- Healthy volunteers
- Not accepted
Summary
This study will investigate the efficacy of the Flutemetamol (18F) Injection PET tracer in identifying abnormal (18F) flutemetamol uptake patterns which predict the conversion from aMCI to a b-amyloid associated clinically probable Alzheimer's disease.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Flutemetamol (18F) Injection | All subjects will receive an i.v. dose of (18F) flutemetamol (less than 10 mg flutemetamol). The nominal activity of a single administration of (18F) flutemetamol will be 185 MBq. |
Timeline
- Start date
- 2009-12-01
- Primary completion
- 2014-01-01
- Completion
- 2014-01-01
- First posted
- 2009-12-09
- Last updated
- 2014-09-11
- Results posted
- 2014-09-11
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01028053. Inclusion in this directory is not an endorsement.