University of Oxford
Oxford, Oxfordshire, United Kingdom
NCT Number: NCT02560610
The aim is to study the effect of OC000459 on eosinophilic airway inflammation and asthma control in subjects with severe, refractory eosinophilic asthma.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Oxford, Oxfordshire, United Kingdom
At week 12 subjects not on oral corticosteroids (OCS) will complete the treatment period and return after 4 weeks for final follow up visit. Those subjects who were taking OCS at baseline will continue for a maximum of 12 additional weeks, double blind period during which their current OCS treatment will be titrated down according to their clinical response.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Mean change from baseline and week 12
Time frame: Every 4 weeks up to week 12
Time frame: At 4,8 and 12 weeks
Time frame: At weeks 4,8 and 12
Time frame: At weeks 4,8 and 12
Chiesi Farmaceutici S.p.A.
Industry
The Effect of OC000459 on Eosinophilic Airway Inflammation and Asthma Control in Subjects With Refractory Eosinophilic Asthma: a Randomised, Double-blind, Placebo Controlled Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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