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Completed Phase 3 Interventional Results available

Study of Ambrisentan in Participants With Pulmonary Hypertension

ClinicalTrials.gov ID: NCT00777920

Public ClinicalTrials.gov record NCT00777920. 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 11, 2026, 9:18 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

ABS-LT: A Phase 3, Long-Term, Open Label, Multicenter Safety Study of Ambrisentan in Subjects With Pulmonary Hypertension

Brief summary

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

The primary objective of this study is to monitor the long-term safety of ambrisentan in adult participants with pulmonary hypertension. The available ambrisentan doses for this study are 2.5, 5, or 10 mg administered orally once daily. Investigators will be able to adjust ambrisentan dose as clinically indicated. A minimum of 4 weeks between dose adjustments is required. Participants receiving other therapies for pulmonary hypertension that are not contraindicated for concomitant use with ambrisentan are permitted to enroll in this study and continue to receive such therapies. Participants enrolled in this study will receive treatment with ambrisentan until such time as the investigator or participant chooses to stop ambrisentan treatment, ambrisentan becomes commercially available, or the sponsor stops the study.

Study identification

NCT ID
NCT00777920
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Gilead Sciences
Industry
Enrollment
140 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Nov 16, 2008
Primary completion
Sep 10, 2019
Completion
Sep 10, 2019
Last update posted
Sep 29, 2020

2008 – 2019

United States locations

U.S. sites
16
U.S. states
13
U.S. cities
13
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Arizona Pulmonary Specialists Phoenix Arizona 85013
University of Colorado Health Science Center Aurora Colorado 80045
University of Connecticut Health Center Farmington Connecticut 06030
Atlanta Institute for Medical Research, Inc. Atlanta Georgia 30030
University of Iowa Iowa City Iowa 52242
Tufts Medical Center Boston Massachusetts 02111
BACH Cardiology/Children's Hospital Boston Massachusetts 02115
Brigham & Women's Hospital Boston Massachusetts 02115
Boston University Medical Center Boston Massachusetts 02118
Washington University Medical Center St Louis Missouri 63110
Newark Beth Israel Medical Center Newark New Jersey 07112
Mary Parkes Asthma Center University of Rochester Rochester New York 14623
University of Pittsburgh Medical Center Presbyterian Pittsburgh Pennsylvania 15213
Rhode Island Hospital Providence Rhode Island 02903
Lexington Pulmonary and Critical Care Medicine Lexington South Carolina 29072

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 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00777920, 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 Sep 29, 2020 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00777920 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →