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Completed Phase 2 Interventional Results available

A Study to Evaluate the Efficacy and Safety of LCI699 Compared to Placebo in Participants With Resistant Hypertension

ClinicalTrials.gov ID: NCT00817635

Public ClinicalTrials.gov record NCT00817635. 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 16, 2026, 6:54 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 Phase II, Randomized, Double-blind, Placebo and Active Controlled, Parallel Group, Multi-center, Dose Ranging Study to Evaluate the Efficacy and Safety of LCI699 Compared to Placebo After 8 Weeks Treatment in Patients With Resistant Hypertension

Study identification

NCT ID
NCT00817635
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis
Industry
Enrollment
155 participants

Conditions and interventions

Conditions

Interventions

  • Eplerenone Drug
  • Eplerenone-matching Placebo Drug
  • LCI699 Drug
  • LCI699-matching Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Dec 21, 2008
Primary completion
Oct 12, 2009
Completion
Oct 12, 2009
Last update posted
Jun 1, 2021

2008 – 2009

United States locations

U.S. sites
37
U.S. states
19
U.S. cities
37
Facility City State ZIP Site status
Horizon Research Group, Inc Mobile Alabama 36608
Cochise Clinical Research Sierra Vista Arizona 85635
Clinical Solutions Advantage Buena Park California 90620
Michael Waldman, MD Irvine California 92618
Long Beach Center for Clinical Research Long Beach California 90806
Clinical Trials Research Roseville California 95661
Orange County Research Center Tustin California 92780
Metro Clinical Research Littleton Colorado 80120
Meridien Research Bradenton Florida 34203
Clinical Research of So. Florida Coral Gables Florida 33134
Jacksonville Heart Center Jacksonville Beach Florida 32250
FPA Clinical Research Kissimmee Florida 34741
Accelovance Melbourne Florida 32935
Cardio-Pulminary Associates Plantation Florida 33317
Meridien Research St. Petersburg Florida 33709
Northwest Clinical Trials Boise Idaho 83704
Provident Clinical Research Addison Illinois 60101
Cedar-Crosse Research Centereet Chicago Illinois 60607
Provident Clinical Research Bloomington Indiana 47403
Accelovance South Bend Indiana 46601
Peter A. Holt Baltimore Maryland 21239
MD Medical Research Oxon Hill Maryland 20745
Chelsea Internal Medicine Chelsea Michigan 48118
New York Cardiovascular Associates New York New York 10001
Charlotte Clinical Research Charlotte North Carolina 28211
Northstate Clinical Research Lenoir North Carolina 28645
Community Research Cincinnati Ohio 45245
Tipton Medical & Diagnostic Center Tipton Pennsylvania 16684
Medical Research South Charleston South Carolina 29407
Mountain View Clinical Research Associates Greer South Carolina 29651
Clinical Research Associates, Inc Nashville Tennessee 37203
Punzi Medical Center Carrollton Texas 75006
KRK Medical Research Dallas Texas 75230
DCOL Center for Clinical Research Longview Texas 75605
Daniel Gottlieb, MD Burien Washington 98166
Rainier Clinical Research Center Renton Washington 98057
Gemini Scientific Madison Wisconsin 83719

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00817635, 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 1, 2021 · Synced May 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00817635 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →