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Examination of the Bronchoprotective Effect of Endothelin Receptor Blockade in Asthma

Examination of the Bronchoprotective Effect of Endothelin Receptor Blockade in Asthma

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01617746
Enrollment
18
Registered
2012-06-12
Start date
2012-11-30
Completion date
2015-12-31
Last updated
2012-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Asthma, Endothelin, Airway hyperreactivity

Brief summary

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.

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.

Interventions

DRUGAmbrisentan

5mg od two weeks

DRUGBosentan

62.5mg bd two weeks

DRUGPlacebo

bd for two weeks

Sponsors

NHS Greater Glasgow and Clyde
CollaboratorOTHER
University of Glasgow
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frameDescription
Difference in doubling dose of methacholine to produce bronchoconstriction compared to placebo2 weeksBoth active treatments will be compared against placebo with respect to protection against methacholine induced bronchoconstriction

Secondary

MeasureTime frameDescription
Which of the endothelin receptors A&B are most bronchoprotective against methacholine2 weeksBoth 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.

Countries

United Kingdom

Contacts

Primary ContactMark Spears, MBChB PhD
mark.spears@glasgow.ac.uk0141 211 1673
Backup ContactRekha Chaudhuri, MD
rekhachaudhuri@yahoo.com0141 211 1673

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026