Safely Change From Bosentan to Ambrisentan in Pulmonary Hypertension

Completed · Phase 4

Conditions studied: Pulmonary Arterial Hypertension

In brief

The primary objective of this study is to assess the safety and tolerance of changing patients currently on bosentan to ambrisentan for the treatment of pulmonary arterial hypertension.

Key facts

Study ID

NCT01330108

Run by

University of Alabama at Birmingham

People needed

32

Starts

2011-05-01

Expected to finish

2012-06-01

Last updated by the study team

2014-08-11

Who can join

Age: 19 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients followed routinely in the pulmonary vascular disease clinic at the University of Alabama in Birmingham, greater than or equal to 19 years of age.
• World Health Organization (WHO) PAH Type I
• WHO class I-IV symptoms (no functional class exclusion).
• On bosentan, twice a day, with a maximum daily dose of 250mg, on a stable dose for 3 months with no clinical indication to discontinue the drug (i.e., increased liver function studies or other intolerance). Patients may be on other drug therapies for PAH, and also may be on oxygen therapy (intermittent or continuous).

You may not qualify if…

• Known intolerance or allergy to ambrisentan.
• Prior therapy with ambrisentan.
• Current therapy with two phosphodiesterase-5 inhibitors.
• Change in other approved therapy for PAH (including phosphodiesterase-5 inhibitors and prostanoids) within 4 weeks of baseline study visit.
• Planned addition of prostanoid for clinical reasons within 3 months of baseline study visit.
• Active participation in another clinical study involving the medical therapy of PAH.
• Uncontrolled systemic hypertension or angina pectoris
• Serum creatinine greater than 2.5 at or within 4 weeks of baseline.
• Serum liver function studies greater than 3 x normal at or within 4 weeks of baseline study visit.
• In the opinion of the investigator, a change in PAH therapy would present significant risk to the subject.
• In the opinion of the investigator, the participant is unlikely to survive for 12 weeks after study entry.
• In the opinion of the investigator, the participant is likely to undergo lung or heart-lung transplantation within 12 weeks of study entry.
• A woman of childbearing potential who is not using an acceptable form of contraception.
• Pregnancy.
• In the opinion of the investigator, a participant who is not capable or willing to follow the study procedures.

Where it is running

• University of Alabama at Birmingham — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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