A 12-week Study Treating Participants Who Have alpha1-antitrypsin-related COPD With Alvelestat (MPH966) or Placebo.
- Conditions
- EmphysemaCOPDAlpha 1-Antitrypsin Deficiency
- Interventions
- Registration Number
- NCT03636347
- Lead Sponsor
- Mereo BioPharma
- Brief Summary
The purpose of this study is to investigate the effect of alvelestat (an oral neutrophil elastase inhibitor) on blood and sputum biomarkers in patients with PiZZ, null or rare variant phenotype/genotype alpha-1 anti-trypsin deficient lung disease. Change in a number of different blood and sputum biomarkers related to lung damage, inflammation and elastase activity will be measured over a 12 week period. The effect on lung function and respiratory symptoms will also be measured.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 99
- Patients with a confirmed diagnosis of alpha-1-anti-trypsin deficiency and a PiZZ, null or other rare geno/phenotype and serum anti-alpha1 antitrypsin levels of less than 11uM
- FEV1 β₯20% predicted
- Computerised tomography (CT) scan evidence of emphysema
- Non-smokers
- Primary diagnosis of bronchiectasis
- An ongoing acute exacerbation of the underlying lung disease
- Underlying liver disease or abnormal liver function tests
- Previous augmentation therapy within 6 months of dosing
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo oral tablet Placebo Oral Tablet - Alvelestat oral tablet - dose 1 Alvelestat oral tablet - dose 1 MPH966 Alvelestat oral tablet - dose 2 Alvelestat oral tablet - dose 2 MPH966
- Primary Outcome Measures
Name Time Method Change from baseline on blood biomarkers of neutrophil elastase activity compared to baseline and placebo 12 weeks Within-individual change from baseline up to end of treatment in:
* Blood neutrophil elastase activity
* Blood AΞ±-Val 360 levels
* Plasma desmosine/isodesmosine levels
- Secondary Outcome Measures
Name Time Method Change from baseline on other blood biomarkers of neutrophil elastase activity 12 weeks Frequency of neutrophil elastase levels below the limit of detection from baseline to end of treatment
Trial Locations
- Locations (26)
UCLA Medical Center
πΊπΈLos Angeles, California, United States
Aarhus Universitetshospital
π©π°Aarhus, Denmark
Lund University Hospital
πΈπͺLund, Sweden
Royal Devon and Exeter NHS Trust
π¬π§Exeter, United Kingdom
University Hospitals Birmingham NHS Foundation Trust
π¬π§Birmingham, United Kingdom
Cambridge University Hospitals Foundation NHS Trust
π¬π§Cambridge, United Kingdom
University of Saskatchewan Royal University Hospital
π¨π¦Saskatoon, Saskatchewan, Canada
UZ Leuven
π§πͺLeuven, Belgium
Gentofte Hospital
π©π°Hellerup, Denmark
Royal Infirmary of Edinburgh
π¬π§Edinburgh, United Kingdom
Hospital Univ Clinico San Carlos
πͺπΈMadrid, Spain
University of Alabama, Birmingham (UAB)
πΊπΈBirmingham, Alabama, United States
PMG Research of Wilmington
πΊπΈWilmington, North Carolina, United States
The University Lung Clinic
π¨π¦Edmonton, Alberta, Canada
Inspiration Research Ltd
π¨π¦Toronto, Ontario, Canada
Hospital Sierrallana
πͺπΈTorrelavega, Spain
Instytut Gruzilicy Chorob Pluc
π΅π±Warsaw, Poland
CTC Gothia Forum Sahlgrenska University Hospital
πΈπͺGothenburg, Sweden
Synddansk Universitet (SDU) - Odense University
π©π°Odense, Denmark
University Hospital Coventry and Warwickshire
π¬π§Coventry, United Kingdom
University Hospitals of Leicester NHS Trust
π¬π§Leicester, United Kingdom
Southampton General Hospital
π¬π§Southampton, United Kingdom
UC Davis Medical Centre
πΊπΈSacramento, California, United States
UZ Gent
π§πͺGent, Belgium
Centre for Heart Lung Innovation, St Pauls Hospital
π¨π¦Vancouver, British Columbia, Canada
Royal Brompton Hospital
π¬π§London, United Kingdom