Status:

COMPLETED

An Efficacy and Safety Study of Galantamine for the Treatment of Patients With Alzheimer's Disease.

Lead Sponsor:

Janssen Pharmaceutical K.K.

Conditions:

Alzheimer Disease

Eligibility:

All Genders

45+ years

Phase:

PHASE3

Brief Summary

The purpose of this study is to evaluate the efficacy and safety of two fixed doses (16mg/day and 24mg/day) of galantamine (a drug for treating dementia) versus placebo for the treatment of patients w...

Detailed Description

This is a randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy and safety of two fixed doses of galantamine (16 and 24 milligrams per day \[mg/day\]) in patients...

Eligibility Criteria

Inclusion

  • Outpatients with a diagnosis of Alzheimer's disease according to the National Institute of Neurological and Communicative Disorders and the Alzheimer's Disease and Related Disorders Association (NINCDS-ADRDA) criteria
  • having a Mini-Mental Status Examination (MMSE) score of 10 - 22 inclusive
  • having an Alzheimer's Disease Assessment Scale - Japan cognitive subscale (ADAS-J cog) score of at least 18
  • exhibiting an onset and progression of cognitive dysfunction during at least 6 months prior to the screening period

Exclusion

  • Patients with neurodegenerative diseases other than Alzheimer's disease, such as Lewy bodies disease, (dementia due to tiny round structures made of proteins that develop within nerve cells in the brain), Parkinsonism, etc
  • Patients with cognitive dysfunction due to cerebral damage resulting from a lack of oxygen, a brain injury, etc
  • Patients with multi-infarct dementia (brought on by a series of strokes) or active cerebrovascular disease
  • Patients with clinically significant cardiovascular disease
  • Patients currently taking drugs such as a cholinesterase inhibitors, which improve cerebral circulation/metabolism

Key Trial Info

Start Date :

April 1 2001

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2004

Estimated Enrollment :

398 Patients enrolled

Trial Details

Trial ID

NCT00301574

Start Date

April 1 2001

End Date

February 1 2004

Last Update

May 17 2011

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