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

NCT01224210 | Completed Phase 3 Results DMC FDA Drug

• 1 other identifier: Ambrisentan Portopulm Study
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 6

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.

Conditions

Portopulmonary Hypertension

Keywords

portopulmonary hypertension; portal hypertension; esophageal or gastric varices; right heart catheterization; transpulmonary gradient; Endothelin Receptor Antagonist; Ambrisentan; Letairis; pulmonary hemodynamics

Outcome Measures

Primary Outcomes (2)

• Change in Pulmonary Vascular Resistance

  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).

  from baseline to Week 24

• 6 Minute Walk Distance

  Change from baseline in 6 Minute Walk Distance to Week 24 for all patients. (difference measured in meters).

  Change from baseline to Week 24

Study Arms (1)

Ambrisentan (24 Weeks), Extension (4 Weeks)

OTHER

Open Label Ambrisentan

Drug: Ambrisentan

Interventions

Ambrisentan DRUG

Ambrisentan once-daily in the morning with or without food. The adult dose selected for this study will be 5 mg for the first 4 weeks. After the initial 4 weeks the dose will be increased to 10mg (available doses are 5, and 10 mg) based on tolerance safety. Subjects will remain on 10mg until they complete the study. Dose adjustments may be made based on side effects.

Also known as: Letairis

Ambrisentan (24 Weeks), Extension (4 Weeks)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Subjects need to fulfill all of the following 4 criteria:
• 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).
• 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
• 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
• Ages 18 years and above

You may not qualify if:

• Presence of any other etiology of pulmonary arterial hypertension (HIV, connective tissue disease, sickle cell, left heart failure, chronic thromboembolic PH, etc)
• Treatment with prostacyclins, other ERAs, or PDE5 inhibitors within 30 days of enrollment.
• Moribund state or anticipated death within 1 month.
• AST or ALT ≥ 5 times upper limit of normal
• Total bilirubin ≥ 3.0 mg/dl
• 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.
• Pregnancy
• Age \<18 years
• Child -Pugh class C

Sponsors & Collaborators

• Tufts Medical Center: lead
• Gilead Sciences: collaborator

Study Sites (6)

UCSD Medical Center

La Jolla, California, 92093, United States

Location

Mayo Clinic Florida

Jacksonville, Florida, 32224, United States

Location

Tufts Medical Center

Boston, Massachusetts, 02111, United States

Location

University of North Carolina

Chapel Hill, North Carolina, 27599, United States

Location

The Ohio State University Medical Center

Columbus, Ohio, 43221, United States

Location

UT Southwestern Medical Center

Dallas, Texas, 75390, United States

Location

Related Publications (1)

• Preston IR, Burger CD, Bartolome S, Safdar Z, Krowka M, Sood N, Ford HJ, Battarjee WF, Chakinala MM, Gomberg-Maitland M, Hill NS. Ambrisentan in portopulmonary hypertension: A multicenter, open-label trial. J Heart Lung Transplant. 2020 May;39(5):464-472. doi: 10.1016/j.healun.2019.12.008. Epub 2020 Jan 21.

  PMID: 32008947 DERIVED

MeSH Terms

Conditions

Hypertension, Portal; Esophageal and Gastric Varices

Interventions

ambrisentan

Condition Hierarchy (Ancestors)

Liver Diseases; Digestive System Diseases; Esophageal Diseases; Gastrointestinal Diseases

Limitations and Caveats

Standardization of the 6 Minute Walk Test

Results Point of Contact

• Title: Ioana Preston MD
• Organization: Tufts Medical Center

ipreston@tuftsmedicalcenter.org

617-636-7609

Study Officials

• Ioana Preston, MD

  Tufts Medical Center

  PRINCIPAL INVESTIGATOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 18, 2010
• First Posted: October 19, 2010
• Study Start: March 1, 2010
• Primary Completion: October 1, 2016
• Study Completion: March 1, 2020
• Last Updated: January 12, 2021
• Results First Posted: January 12, 2021

Record last verified: 2020-12

Data Sharing

• IPD Sharing: Will not share

Locations

US (6)