Ambrisentan in Patients With Porto-pulmonary Hypertension A Multicenter Open Label Trial

Phase 3

Completed

• Conditions: Portopulmonary Hypertension
• Interventions: Drug: Ambrisentan

• Registration Number: NCT01224210
• Lead Sponsor: Tufts Medical Center

Brief Summary

This is an Open Label, Multicenter, pilot clinical trial to assess the efficacy and safety of an oral selective Endothelin Receptor Antagonist (ambrisentan) in patients with portopulmonary hypertension.

Preliminary evidence suggests that ambrisentan is safe and effective in patients with portopulmonary hypertension. The goal of therapy for these patients is to improve symptoms of dyspnea and to improve pulmonary hemodynamics to a mean pulmonary artery pressure \<35 mm Hg in order to make patients eligible for liver transplantation. Therefore, the primary endpoints for this study will include 6 minute walk distance (6MWD) and pulmonary vascular resistance (PVR).

Eligible subjects will receive 5 mg ambrisentan once-daily for the first 4 weeks. After the initial 4-week period, investigators will increase study drug dose to 10 mg once daily (both 5 mg and 10 mg doses are FDA approved). If 10 mg is not tolerated in the opinion of investigator, then the investigator may decrease the dose back to 5 mg once daily. Primary outcome is a change in both the 6 Minute Walk Distance and in Pulmonary Vascular Resistance from baseline to Week 24. Subjects will be monitored with liver function tests (LFT) every 2 weeks for the first 8 weeks, then every 4 weeks thereafter. These safety laboratory tests may be performed at a local phlebotomy laboratory or at the Investigator clinic. In addition, the Investigator will assess each subject for safety and efficacy at Week 4, Week 12, and Week 24. Following Week 24, subjects will be assessed for safety and efficacy every 12 weeks. Patients will be followed for a total of 1 year. After 1 year, if the Investigator feels that continuing the treatment will be beneficial to the patients, they will be provided with ambrisentan by Gilead Pharmaceuticals, free of charge.

Detailed Description

Not available

Study Timeline

• Study Start: 2010-03
• Study First Submitted: 2010-10-18
• Study First Submitted QC: 2010-10-18
• Study First Posted: 2010-10-19
• Primary Completion: 2016-10
• Study Completion: 2020-03
• Results First Submitted: 2020-09-01
• Status Verified: 2020-12
• Results First Submitted QC: 2020-12-16
• Last Update Submitted: 2020-12-16
• Results First Posted: 2021-01-12
• Last Update Posted: 2021-01-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Subjects need to fulfill all of the following 4 criteria:

1. Evidence of portal hypertension (by hemodynamic measurement, or by Doppler flow of portal circulation, or by clinical evidence of portal hypertension such as esophageal or gastric varices, as evidenced by prior upper endoscopy).

2. Evidence of pulmonary arterial hypertension by right heart catheterization (all three criteria need to be present) Right heart catheterization may have been performed up to 30 days prior to screening

   • Mean PAP (pulmonary artery pressure) >25 mm Hg, and
   • PVR (pulmonary vascular resistance) >240 dynes/s/cm5, and
   • TPG (transpulmonary gradient = meanPAP -PAWP) >12 mm Hg

3. Baseline AST, ALT < 5 times the upper limit of normal, total Bili < 3.0 mg/dl, and mild liver impairment with Child -Pugh class A or B

4. Ages 18 years and above

Exclusion Criteria

1. Presence of any other etiology of pulmonary arterial hypertension (HIV, connective tissue disease, sickle cell, left heart failure, chronic thromboembolic PH, etc)
2. Treatment with prostacyclins, other ERAs, or PDE5 inhibitors within 30 days of enrollment.
3. Moribund state or anticipated death within 1 month.
4. AST or ALT ≥ 5 times upper limit of normal
5. Total bilirubin ≥ 3.0 mg/dl
6. Significant lung disease (obstructive lung disease with FEV1 < 1L, or FEV1/FVC <50%; or restrictive lung disease with Total Lung Capacity < 60% predicted). PFTs may have been performed up to 6 months prior to enrollment.
7. Pregnancy
8. Age <18 years
9. Child -Pugh class C

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Ambrisentan (24 Weeks), Extension (4 Weeks)	Ambrisentan	Open Label Ambrisentan

Primary Outcome Measures

Name	Time	Method
Change in Pulmonary Vascular Resistance	from baseline to Week 24	Change in Pulmonary Vascular Resistance from baseline to Week 24 for all patients (using cardiac output \[CO\] measured by the thermodilution method and reported as percent difference from baseline).
6 Minute Walk Distance	Change from baseline to Week 24	Change from baseline in 6 Minute Walk Distance to Week 24 for all patients. (difference measured in meters).

Trial Locations

Locations (6)

UCSD Medical Center; 🇺🇸 La Jolla, California, United States

University of North Carolina; 🇺🇸 Chapel Hill, North Carolina, United States

The Ohio State University Medical Center; 🇺🇸 Columbus, Ohio, United States

Mayo Clinic Florida; 🇺🇸 Jacksonville, Florida, United States

Tufts Medical Center; 🇺🇸 Boston, Massachusetts, United States

UT Southwestern Medical Center; 🇺🇸 Dallas, Texas, United States