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Completed Phase 1 Interventional

A Study to Assess the Effects of Naproxcinod and Naproxen on Blood Pressure Measurements in Osteoarthritis Patients With Controlled High Blood Pressure

ClinicalTrials.gov ID: NCT00662610

Public ClinicalTrials.gov record NCT00662610. 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 4, 2026, 5:19 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 12-Week, Phase 1, Multicenter, Double-Blind, Randomized, Dose Ranging, Forced Titration, Naproxen-Controlled, Parallel-Group, Pharmacodynamic Study, to Assess the Effects Different Doses of Naproxcinod and Naproxen on Arterial Blood Pressure as Measured by Ambulatory Blood Pressure Monitoring in Osteoarthritis Patients With Controlled Essential Hypertension

Study identification

NCT ID
NCT00662610
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
NicOx
Industry
Enrollment
120 participants

Conditions and interventions

Interventions

  • naproxcinod 375 mg -750 mg -1125 mg bid Drug
  • naproxen 250 mg - 500mg -750 mg bid Drug

Drug

Eligibility (public fields only)

Age range
40 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 29, 2008
Primary completion
Jul 31, 2008
Completion
Oct 31, 2008
Last update posted
Jun 16, 2011

2008

United States locations

U.S. sites
29
U.S. states
21
U.S. cities
29
Facility City State ZIP Site status
Not listed Mobile Alabama
Not listed Tempe Arizona
Not listed Tucson Arizona
Not listed Beverly Hills California
Not listed Buena Park California
Not listed Colorado Springs Colorado
Not listed Boynton Beach Florida
Not listed Stockbridge Georgia
Not listed Boise Idaho
Not listed Chicago Illinois
Not listed Evansville Indiana
Not listed Newburgh Indiana
Not listed Terre Haute Indiana
Not listed Louisville Kentucky
Not listed New Orleans Louisiana
Not listed Billings Montana
Not listed Las Vegas Nevada
Not listed Edison New Jersey
Not listed Binghamton New York
Not listed Johnson City New York
Not listed Winston-Salem North Carolina
Not listed Cleveland Ohio
Not listed Duncansville Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Clarksville Tennessee
Not listed Austin Texas
Not listed Dallas Texas
Not listed Houston Texas
Not listed Norfolk Virginia

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00662610, 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 16, 2011 · Synced May 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00662610 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →