Examination of the Bronchoprotective Effect of Endothelin Receptor Blockade in Asthma

The purpose of this study will be to determine if blockade of endothelin 1 signalling via endothelin receptor A using ambrisentan or dual blockade (A&B) via bosentan can provide protection against methacholine induced bronchoconstriction in asthma.

Study Overview

• Status: Unknown
• Conditions: Asthma
• Intervention / Treatment: Drug: Ambrisentan; Drug: Bosentan; Drug: Placebo

Detailed Description

Endothelin 1 may have a role in the development of acute airway narrowing in asthma. Blockade of the endothelin system may thereby protect against airway narrowing. Two receptors exist for endothelin 1, Endothelin A & B. Both can be blocked by Bosentan, and the A receptor by ambrisentan. Both medications are currently in use for the treatment of pulmonary arterial hypertension. The investigators will endeavour to examine the potential role of endothelin 1 in the development of airway narrowing in asthma through blockade of the endothelin receptors A&B through the use of bosentan and ambrisentan.

• Study Type: Interventional
• Enrollment (Anticipated): 18
• Phase: Phase 2

Contacts and Locations

Study Locations

• United Kingdom
  • Glasgow, United Kingdom, G12 0YN
    • Asthma Research Unit, University of Glasgow

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 60 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Physician diagnosis of asthma confirmed objectively by airway hyperactivity to methacholine (as determined by a ≥ 20% drop in FEV at a methacholine dose of ≤ 8mg/ml after β-agonist withdrawal as per ATS guidelines)
2. Age range 18-60 years
3. FEV1 ≥ 60% predicted
4. Duration of asthma > 6 months and on stable medication for 4 weeks
5. Prescribed and compliant with inhaled corticosteroid up to a maximum of 2000mcg beclomethasone or equivalent
6. No history of previous regular smoking and current non-smoker

Exclusion Criteria:

1. Unstable asthma; defined as the presence of 1 or more of the following events in the month prior to study [Emergency/'out of hours' visit to GP for asthma exacerbation; GP visit to patient at home for asthma exacerbation or A & E/hospital admission for asthma exacerbation]
2. Treatment with oral corticosteroids in the past month
3. Need for maintenance oral corticosteroid therapy
4. Pregnancy or planning to become pregnant over course of study and up to one month after

5. Excessive risk of hepatotoxicity from endothelin receptor antagonists;

   • Alcohol excess (defined as regular consumption above government daily recommend limits; currently defined as 28 units per wk for men, 21 units per week for women)
   • Previous intravenous drug use
   • Current or known history of liver disease (with the exception of Gilberts disease and gallstones)
   • Chronic hepatitis (either viral (e.g. hepatitis B or C) or autoimmune)
   • Bilirubin, alanine aminotransferase (ALT) or asparate aminotransferase (AST) greater than the upper limit of normal at screening
6. Anaemia (defined as haemoglobin below the lower reference range for sex) at screening
7. Renal failure (defined as eGFR less than 50 mL/minute/1.73 m2) at screening
8. Known HIV positivity
9. History of inability to tolerate bosentan or ambrisentan
10. Significant medical conditions other than asthma felt by investigator to preclude participation in study. This could be either in patients best interest or due to potential to significantly alter responses to medication and hence alter power of clinical trial (examples include; significant heart failure (NYHA grades II-IV), diabetes mellitus, bronchiectasis or haematological malignancy).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: Quadruple

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: Placebo	Drug: Placebo; bd for two weeks
Experimental: Ambrisentan; 5mg od ambrisentan	Drug: Ambrisentan; 5mg od two weeks; Other Names: Volibris
Experimental: Bosentan; 62.5mg bosentan	Drug: Bosentan; 62.5mg bd two weeks; Other Names: Tracleer

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Difference in doubling dose of methacholine to produce bronchoconstriction compared to placebo	Both active treatments will be compared against placebo with respect to protection against methacholine induced bronchoconstriction	2 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Which of the endothelin receptors A&B are most bronchoprotective against methacholine	Both bostentan and ambrisentans effect on airway response to methacholine will be compared to placebo. The relative efficacy will be compared, in terms of doubling doses of methacholine.	2 weeks

Collaborators and Investigators

• Sponsor: University of Glasgow
• Collaborators: NHS Greater Glasgow and Clyde
• Investigators: Principal Investigator: Mark Spears, MBChB PhD, University of Glasgow

Study record dates

Study Major Dates

• Study Start: November 1, 2012
• Primary Completion (Anticipated): May 1, 2014
• Study Completion (Anticipated): December 1, 2015

Study Registration Dates

• First Submitted: March 7, 2012
• First Submitted That Met QC Criteria: June 10, 2012
• First Posted (Estimate): June 12, 2012

Study Record Updates

• Last Update Posted (Estimate): June 12, 2012
• Last Update Submitted That Met QC Criteria: June 10, 2012
• Last Verified: June 1, 2012

More Information

Terms related to this study

• Keywords: Asthma; Endothelin; Airway hyperreactivity
• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Immune System Diseases; Lung Diseases; Hypersensitivity, Immediate; Bronchial Diseases; Lung Diseases, Obstructive; Respiratory Hypersensitivity; Hypersensitivity; Asthma; Molecular Mechanisms of Pharmacological Action; Antihypertensive Agents; Endothelin Receptor Antagonists; Bosentan; Ambrisentan
• Other Study ID Numbers: AR012