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Completed Phase 3 Interventional Results available

A Study of First-Line Ambrisentan and Tadalafil Combination Therapy in Subjects With Pulmonary Arterial Hypertension (PAH)

ClinicalTrials.gov ID: NCT01178073

Public ClinicalTrials.gov record NCT01178073. 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 17, 2026, 9:37 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

AMBITION: A Randomised, Multicenter Study of First-Line Ambrisentan and Tadalafil Combination Therapy in Subjects With Pulmonary Arterial Hypertension (PAH)

Brief summary

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

The purpose of this study is to compare the two treatment strategies; first-line combination therapy (ambrisentan and tadalafil) versus first-line monotherapy (ambrisentan or tadalafil) in subjects with Pulmonary Arterial Hypertension. This will be assessed by time to the first clinical failure event.

Study identification

NCT ID
NCT01178073
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
610 participants

Conditions and interventions

Interventions

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
Oct 1, 2010 (Type not available)
Primary completion
Jul 31, 2014 (Actual)
Completion
Jul 31, 2014 (Actual)
Last update posted
Sep 13, 2017

2010 – 2014

United States locations

U.S. sites
61
U.S. states
29
U.S. cities
53
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Mobile Alabama 36617 —
GSK Investigational Site Phoenix Arizona 85012 —
GSK Investigational Site Tucson Arizona 85724 —
GSK Investigational Site La Jolla California 92093 —
GSK Investigational Site Los Angeles California 90073 —
GSK Investigational Site Sacramento California 95817 —
GSK Investigational Site Torrance California 90502 —
GSK Investigational Site Aurora Colorado 80045 —
GSK Investigational Site Gainesville Florida 32610 —
GSK Investigational Site Jacksonville Florida 32209 —
GSK Investigational Site Kissimmee Florida 34741 —
GSK Investigational Site Orlando Florida 32803 —
GSK Investigational Site Weston Florida 33331 —
GSK Investigational Site Atlanta Georgia 30322 —
GSK Investigational Site Decatur Georgia 30030 —
GSK Investigational Site Oakbrook Terrace Illinois 60181 —
GSK Investigational Site Carmel Indiana 46032 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Portland Maine 04102 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Boston Massachusetts 02111 —
GSK Investigational Site Boston Massachusetts 02115 —
GSK Investigational Site Boston Massachusetts 02118 —
GSK Investigational Site Springfield Massachusetts 01199 —
GSK Investigational Site Ann Arbor Michigan 48109 —
GSK Investigational Site Detroit Michigan 48201 —
GSK Investigational Site Troy Michigan 48085 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site Morristown New Jersey 07962 —
GSK Investigational Site Newark New Jersey 07112 —
GSK Investigational Site New Hyde Park New York 11040 —
GSK Investigational Site New York New York 10003 —
GSK Investigational Site New York New York 10019 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site New York New York 10032 —
GSK Investigational Site Rochester New York 14623 —
GSK Investigational Site Asheville North Carolina 28803 —
GSK Investigational Site Chapel Hill North Carolina 27599 —
GSK Investigational Site Cincinnati Ohio 45219 —
GSK Investigational Site Cincinnati Ohio 45267 —
GSK Investigational Site Cleveland Ohio 44195 —
GSK Investigational Site Columbus Ohio 43221 —
GSK Investigational Site Portland Oregon 97220 —
GSK Investigational Site Philadelphia Pennsylvania 19104 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Pittsburgh Pennsylvania 15212 —
GSK Investigational Site Pittsburgh Pennsylvania 15213 —
GSK Investigational Site Providence Rhode Island 02903 —
GSK Investigational Site Nashville Tennessee 37232 —
GSK Investigational Site Dallas Texas 75390 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Temple Texas 76508 —
GSK Investigational Site Murray Utah 84157 —
GSK Investigational Site Charlottesville Virginia 22908 —
GSK Investigational Site Norfolk Virginia 23507 —
GSK Investigational Site Richmond Virginia 23298 —
GSK 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 82 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01178073, 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 13, 2017 · Synced Oct 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01178073 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →