ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Safety and Efficacy of Aliskiren in Pediatric Hypertensive Patients 6-17 Years of Age

ClinicalTrials.gov ID: NCT01150357

Public ClinicalTrials.gov record NCT01150357. 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 18, 2026, 11:20 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 Multicenter, Randomized, Double-blind, 8 Week Study to Evaluate the Dose Response, Efficacy and Safety of Aliskiren in Pediatric Hypertensive Patients 6-17 Years of Age

Study identification

NCT ID
NCT01150357
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
267 participants

Conditions and interventions

Conditions

Interventions

  • Aliskiren (150/300/600 mg) Drug
  • Aliskiren (37.5/75/150 mg) Drug
  • Aliskiren (6.25/12.5/25 mg) Drug

Drug

Eligibility (public fields only)

Age range
6 Years to 17 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
May 31, 2010
Primary completion
Jul 31, 2014
Completion
Jul 31, 2014
Last update posted
Oct 14, 2015

2010 – 2014

United States locations

U.S. sites
23
U.S. states
18
U.S. cities
22
Facility City State ZIP Site status
Novartis Investigative Site Birmingham Alabama 35294-0006
Novartis Investigative Site Little Rock Arkansas 72202
Novartis Investigative Site Los Angeles California 90048
Novartis Investigative Site San Diego California 92123
Novartis Investigative Site Pensacola Florida 32504
Novartis Investigative Site Atlanta Georgia 30322
Novartis Investigative Site Dalton Georgia 30721
Novartis Investigative Site Lewiston Idaho 83501
Novartis Investigative Site Park Ridge Illinois 60068
Novartis Investigative Site Louisville Kentucky 40202
Novartis Investigative Site Hattiesburg Mississippi 39401
Novartis Investigative Site Jackson Mississippi 39209
Novartis Investigative Site Hackensack New Jersey 07601
Novartis Investigative Site New York New York 10016
Novartis Investigative Site Columbus Ohio 43205
Novartis Investigative Site Toledo Ohio 43606
Novartis Investigative Site Portland Oregon 97225
Novartis Investigative Site Portland Oregon 97239
Novartis Investigative Site Pittsburgh Pennsylvania 15224
Novartis Investigative Site Charleston South Carolina 29425
Novartis Investigative Site Amarillo Texas 79106
Novartis Investigative Site Seattle Washington 98105
Novartis Investigative Site Charleston West Virginia 25304

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 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01150357, 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 Oct 14, 2015 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01150357 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →