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Terminated Phase 3 Interventional Results available

Sitaxsentan Efficacy And Safety Trial With A Randomized Prospective Assessment Of Adding Sildenafil (SR-PAAS)

ClinicalTrials.gov ID: NCT00795639

Public ClinicalTrials.gov record NCT00795639. 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, 2:29 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 Phase 3, Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Safety And Efficacy Study Of Sitaxsentan Sodium In Subjects With Pulmonary Arterial Hypertension

Brief summary

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

This protocol is for subjects with pulmonary arterial hypertension and is the first of 3 studies forming the Sitaxsentan efficacy and safety trial with Randomized Prospective Assessment of Adding Sildenafil (SR-PAAS) program.

Study identification

NCT ID
NCT00795639
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
183 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 Years to 80 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 2008 (Type not available)
Primary completion
Mar 2011 (Actual)
Completion
Mar 2011 (Actual)
Last update posted
Mar 24, 2015

2008 – 2011

United States locations

U.S. sites
32
U.S. states
18
U.S. cities
31
Facility City State ZIP Site status
Pfizer Investigational Site Fountain Valley California 92708 —
Pfizer Investigational Site Mather California 95655 —
Pfizer Investigational Site Sacramento California 95817 —
Pfizer Investigational Site Englewood Colorado 80113 —
Pfizer Investigational Site Littleton Colorado 80120 —
Pfizer Investigational Site Gainesville Florida 32610 —
Pfizer Investigational Site Sarasota Florida 34233 —
Pfizer Investigational Site Weston Florida 33331 —
Pfizer Investigational Site Chicago Illinois 60612 —
Pfizer Investigational Site Olathe Kansas 66061 —
Pfizer Investigational Site Towson Maryland 21204 —
Pfizer Investigational Site Boston Massachusetts 02111 —
Pfizer Investigational Site Omaha Nebraska 68131 —
Pfizer Investigational Site New Brunswick New Jersey 08903 —
Pfizer Investigational Site Islandia New York 11749 —
Pfizer Investigational Site Stony Brook New York 11794 —
Pfizer Investigational Site Chapel Hill North Carolina 27599 —
Pfizer Investigational Site Cincinnati Ohio 45219 —
Pfizer Investigational Site Cleveland Ohio 44106 —
Pfizer Investigational Site Lancaster Pennsylvania 17602 —
Pfizer Investigational Site Lancaster Pennsylvania 17603 —
Pfizer Investigational Site Philadelphia Pennsylvania 19140 —
Pfizer Investigational Site Pittsburgh Pennsylvania 15212 —
Pfizer Investigational Site Providence Rhode Island 02903 —
Pfizer Investigational Site Charleston South Carolina 29425 —
Pfizer Investigational Site Dallas Texas 75390 —
Pfizer Investigational Site Houston Texas 77030 —
Pfizer Investigational Site San Antonio Texas 78229 —
Pfizer Investigational Site Temple Texas 76508 —
Pfizer Investigational Site Lynchburg Virginia 24501 —
Pfizer Investigational Site Richmond Virginia 23225 —
Pfizer Investigational Site Milwaukee Wisconsin 53215 —

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 53 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00795639, 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 Mar 24, 2015 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00795639 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →