ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Safety and Efficacy of Aliskiren on the Progression of Atherosclerosis in Coronary Artery Disease Patients

ClinicalTrials.gov ID: NCT00853827

Public ClinicalTrials.gov record NCT00853827. 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 May 11, 2026, 8:37 AM 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 104 Week, Randomized, Double Blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy of Aliskiren on the Progression of Atherosclerosis in Patients With Coronary Artery Disease When Added to Optimal Background Therapy

Study identification

NCT ID
NCT00853827
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
613 participants

Conditions and interventions

Interventions

  • Aliskiren Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
35 Years and older
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
Feb 28, 2009
Primary completion
Dec 31, 2012
Completion
Dec 31, 2012
Last update posted
Jun 2, 2014

2009 – 2013

United States locations

U.S. sites
54
U.S. states
27
U.S. cities
51
Facility City State ZIP Site status
Novartis Investigative Site Mobile Alabama 36693
Novartis Investigative Site Phoenix Arizona 85054
Novartis Investigative Site Tucson Arizona 85723-0001
Novartis Investigative Site Tucson Arizona 85745
Novartis Investigative Site Los Angeles California 90033
Novartis Investigative Site Los Angeles California 90095
Novartis Investigative Site San Diego California 92161
Novartis Investigative Site Stockton California 95204
Novartis Investigative Site Torrance California 90502
Novartis Investigative Site Boulder Colorado 80304
Novartis Investigative Site Farmington Connecticut 06030-3100
Novartis Investigative Site Washington D.C. District of Columbia 20010
Novartis Investigative Site Washington D.C. District of Columbia 20037
Novartis Investigative Site Gainesville Florida 32610
Novartis Investigative Site Hudson Florida 34667
Novartis Investigative Site Miami Florida 33137-3732
Novartis Investigative Site Port Charlotte Florida 33952
Novartis Investigative Site Safety Harbor Florida 34695
Novartis Investigative Site Decatur Georgia 30033
Novartis Investigative Site Elkhart Indiana 46514
Novartis Investigative Site Lexington Kentucky 40536
Novartis Investigative Site Louisville Kentucky 40202
Novartis Investigative Site Covington Louisiana 70433
Novartis Investigative Site Columbia Maryland 21044
Novartis Investigative Site Boston Massachusetts
Novartis Investigative Site Flint Michigan 48532
Novartis Investigative Site Kalamazoo Michigan 49048
Novartis Investigative Site Midland Michigan 48640
Novartis Investigative Site Petoskey Michigan 49770
Novartis Investigative Site Saginaw Michigan 48601
Novartis Investigative Site Rochester Minnesota 55905-0001
Novartis Investigative Site Saint Paul Minnesota 55102
Novartis Investigative Site Columbia Missouri 65212
Novartis Investigative Site Ridgewood New Jersey 07450
Novartis Investigative Site Albuquerque New Mexico 87131-5271
Novartis Investigative Site Buffalo New York 14215
Novartis Investigative Site New York New York 10011
Novartis Investigative Site Syracuse New York 13210-1640
Novartis Investigative Site Williamsville New York 14221
Novartis Investigative Site Raleigh North Carolina 27610
Novartis Investigative Site Fargo North Dakota 58122
Novartis Investigative Site Cleveland Ohio 44109-1998
Novartis Investigative Site Oklahoma City Oklahoma 73109
Novartis Investigative Site Tulsa Oklahoma 74104-4243
Novartis Investigative Site Bend Oregon 97701
Novartis Investigative Site Hillsboro Oregon 97123
Novartis Investigative Site Danville Pennsylvania 17822-2001
Novartis Investigative Site Pittsburgh Pennsylvania 15213
Novartis Investigative Site Johnson City Tennessee 37604
Novartis Investigative Site Memphis Tennessee 38104
Novartis Investigative Site Oak Ridge Tennessee 37830
Novartis Investigative Site Dallas Texas 75226
Novartis Investigative Site Katy Texas 77493
Novartis Investigative Site San Antonio Texas 78229-3900

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 75 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00853827, 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 Jun 2, 2014 · Synced May 11, 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 protocol, eligibility criteria, and contact information for NCT00853827 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →