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Completed Phase 3 Interventional Results available

Comparative Efficacy, Safety, and Tolerability of Rivastigmine 10 and 15 cm^2 Patch in Patients With Alzheimer's Disease (AD) Showing Cognitive Decline

ClinicalTrials.gov ID: NCT00506415

Public ClinicalTrials.gov record NCT00506415. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 12:30 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 48-Week, Multicenter, Randomized, Double-Blind, Parallel-Group Evaluation of the Comparative Efficacy, Safety, and Tolerability of Exelon® 10 and 15 cm^2 Patch in Patients With Mild to Moderate Alzheimer's Disease (AD) Showing Functional and Cognitive Decline

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study was to support the optimal use of rivastigmine patch in long-term treatment of Alzheimer's Disease in patients demonstrating functional and cognitive decline at the target maintenance dose of rivastigmine patch 10 cm\^2.

Study identification

NCT ID
NCT00506415
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
1,584 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2007 (Type not available)
Primary completion
May 2011 (Actual)
Completion
May 2011 (Actual)
Last update posted
Sep 19, 2012

2007 – 2011

United States locations

U.S. sites
65
U.S. states
22
U.S. cities
64
Facility City State ZIP Site status
Novartis investigative site Birmingham Alabama 35294 —
Novartis investigative site Gilbert Arizona 85234 —
Novartis investigative site Phoenix Arizona 85004 —
Novartis investigative site Sun City Arizona 85351 —
Novartis investigative site Anaheim California 92804 —
Novartis investigative site Carson California 90746 —
Novartis investigative site Costa Mesa California 92626 —
Novartis investigative site Fullerton California 92835 —
Novartis investigative site La Habra California 90631 —
Novartis investigative site La Jolla California 92037 —
Novartis investigative site National City California 91950 —
Novartis investigative site Redlands California 92374 —
Novartis investigative site San Francisco California 94115 —
Novartis investigative site Fort Collins Colorado 80524 —
Novartis investigative site Longmont Colorado 80501 —
Novartis investigative site Boca Raton Florida 33431 —
Novartis investigative site Bradenton Florida 32405 —
Novartis investigative site Deerfield Beach Florida 33064 —
Novartis investigative site Delray Beach Florida 33445 —
Novartis investigative site Fort Lauderdale Florida 33308 —
Novartis investigative site Gainesville Florida 32610 —
Novartis investigative site Miami Beach Florida 33140 —
Novartis investigative site Pompano Beach Florida 33060 —
Novartis investigative site Port Charlotte Florida 33952 —
Novartis investigative site Sunrise Florida 33351 —
Novartis investigative site West Palm Beach Florida 33407 —
Novartis investigative site Atlanta Georgia 30341-4155 —
Novartis investigative site Macon Georgia 31201 —
Novartis Investigative Site Honolulu Hawaii 96817 —
Novartis investigative site Chicago Illinois 60611 —
Novartis investigative site Springfield Massachusetts 01104 —
Novartis investigative site Flint Michigan 48532 —
Novartis investigative site Flushing Michigan 48433 —
Novartis investigative site Roseville Michigan 48066 —
Novartis investigative site Traverse City Michigan 49684-2340 —
Novartis investigative site Hattiesburg Mississippi 39401 —
Novartis investigative site Ocean Springs Mississippi 39564 —
Novartis investigative site Columbia Missouri 65201 —
Novartis investigative site St Louis Missouri 63141 —
Novartis investigative site Flemington New Jersey 08822 —
Novartis investigative site Nutley New Jersey 07110 —
Novartis investigative site Somerset New Jersey 08873 —
Novartis investigative site Albany New York 12208 —
Novartis investigative site Syracuse New York 13210-1853 —
Novartis investigative site Greensboro North Carolina 27401 —
Novartis investigative site Morganton North Carolina 28655 —
Novartis investigative site Winston-Salem North Carolina 27103-4019 —
Novartis investigative site Winston-Salem North Carolina 27103 —
Novartis investigative site Canton Ohio 44718 —
Novartis investigative site Columbus Ohio 43220 —
Novartis investigative site Corvallis Oregon 97330 —
Novartis investigative site Portland Oregon 97225 —
Novartis investigative site Beaver Pennsylvania 15009-1957 —
Novartis investigative site Erie Pennsylvania 16506 —
Novartis investigative site Greensburg Pennsylvania 15601 —
Novartis investigative site Pittsburgh Pennsylvania 15243 —
Novartis investigative site Beaufort South Carolina 29902 —
Novartis investigative site Summerville South Carolina 29485 —
Novartis investigative site Brentwood Tennessee 37027-5240 —
Novartis investigative site Nashville Tennessee 37203 —
Novartis investigative site Dallas Texas 75231 —
Novartis investigative site Fort Worth Texas 76107 —
Novartis investigative site Irving Texas 75062 —
Novartis investigative site Charleston West Virginia 25304 —
Novartis investigative site Huntington West Virginia 25701 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 79 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00506415, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 19, 2012 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00506415 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →