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Completed Phase 3 Interventional Results available

BAY63-2521:Long-term Extension Study in Patients With Pulmonary Arterial Hypertension

ClinicalTrials.gov ID: NCT00863681

Public ClinicalTrials.gov record NCT00863681. 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 Sep 5, 2026, 12:34 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

Long-term Extension, Multicentre, Multi-national Study to Evaluate the Safety and Tolerability of Oral BAY63-2521 (1mg,1.5 mg, 2.0 mg, 2.5 mg Tid) in Patients With Symptomatic Pulmonary Arterial Hypertension (PAH)

Brief summary

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

Patients who have completed the 12 weeks treatment of the PATENT-1 trial (study number 12934) will be asked to participate in this long term extension study with BAY63-2521.

Study identification

NCT ID
NCT00863681
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
396 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Mar 11, 2009
Primary completion
Aug 18, 2019
Completion
Aug 18, 2019
Last update posted
Nov 6, 2023

2009 – 2019

United States locations

U.S. sites
11
U.S. states
6
U.S. cities
10
Facility City State ZIP Site status
Not listed Los Angeles California 90073
Not listed Sacramento California 95817
Not listed Aurora Colorado 80045
Not listed Boston Massachusetts 02111
Not listed Boston Massachusetts 02114
Not listed Omaha Nebraska 68131
Not listed Cleveland Ohio 44195
Not listed Columbus Ohio 43221
Not listed Fairfield Ohio 45014
Not listed Dallas Texas 75390-9252
Not listed El Paso Texas 79902

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 88 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00863681, 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 Nov 6, 2023 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00863681 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →