NCT Number: NCT00083421
Effects of ONO-2506PO in Patients With Alzheimer's Disease
The purpose of this study is to establish the presence of an effect of treatment with ONO-2506PO in patients with Alzheimer's Disease, based upon cognitive and global scales.
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Notify MeKey information
Conditions
Age range
50 year–90 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
Inova Health Research, Inc., Kelowna, British Columbia, Canada
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Diagnosis of probable Alzheimer's Disease using NINCDS/ADRDA criteria
- Standardized MMSE Score of 13 to 24 points (inclusive)
- Modified Hachinski score equal or less than 4
Exclusion criteria
- Serious systemic disease that may preclude survival to study completion
- Other illnesses that may include dementive features
Treatment and study plan
Primary outcomes
-
Cognitive Function Scale
-
Global Function Scale
Secondary outcomes
-
ADL Scale
-
Psychiatric Symptom Scale
Sponsors and collaborators
Lead sponsor
Ono Pharma USA Inc
Industry
Registry information
Important dates
- Study start
- 2004
- Study completion
- 2007
- First posted
- Jun 18, 2004
- Registry last updated
- Jun 13, 2012
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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