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Completed

NCT Number: NCT02560610

Effect of OC000459 on Eosinophilic Airway Inflammation in Severe Asthma

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

University of Oxford

Oxford, Oxfordshire, United Kingdom

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Show evidence of reversible airflow obstruction documented within the previous 12 months or prior to Randomisation.
  • Meet the European Respiratory Society/American Thoracic Society (ERS/ATS) criteria for severe asthma at Screening.
  • Have documented evidence of eosinophilic airway inflammation during the 12 months prior to Screening.
  • Have evidence of eosinophilic airway inflammation at Screening as reflected by an induced sputum eosinophil count of ≥3%.
  • Subjects who are taking oral corticosteroids (OCS) must be receiving a 20 mg prednisolone equivalent dose, or less, daily for at least four weeks before the first dose of study drug. The dose of OCS should be unchanged for at least 14 days prior to the Baseline visit.

Exclusion criteria

  • Treatment with XolairTM or anti-Th2 biologicals within 6 months prior to screening.
  • Subjects with clinically significant abnormal serum biochemistry, haematology and urine examination values
  • Subjects who have been hospitalised in the last 3 months.
  • History of more than 2 episodes of confirmed bacterial lower respiratory tract infection or current lower respiratory tract infection.
  • Subjects are current smokers or have a smoking history of >15 pack years.
  • Significant comorbidity that in the Investigator's opinion is likely to impact the subject's participation in a 26 week study.
  • Presence of a clinically important lung condition other than asthma, malignancy or previous history of cancer in remission for less than 12 months, clinically important liver or kidney disease, uncontrolled clinically significant cardiovascular disease, hypereosinophilic syndromes such as Churg-Strauss Syndrome or eosinophilic oesophagitis.

Treatment and study plan

OC000459

Drug

Placebo

Drug

Primary outcomes

  1. Compare the effect of OC000459 50mg given once daily with placebo on the induced sputum eosinophil counts.

    Time frame: Mean change from baseline and week 12

Secondary outcomes

  1. The effect on pre- and post-bronchodilator spirometry using forced expiratory volume in one second (FEV1).

    Time frame: Every 4 weeks up to week 12

  2. The effect of OC000459 on fractional exhaled nitric oxide (FeNO).

    Time frame: At 4,8 and 12 weeks

  3. Measuring quality of life using standardised asthma quality of life questionnaire (AQLQ(S)).

    Time frame: At weeks 4,8 and 12

  4. Statistical comparison from baseline on induced sputum eosinophil count.

    Time frame: At weeks 4,8 and 12

Sponsors and collaborators

Lead sponsor

Chiesi Farmaceutici S.p.A.

Industry

Collaborators

  • Atopix Therapeutics, Ltd.

Registry information

Official study title

The Effect of OC000459 on Eosinophilic Airway Inflammation and Asthma Control in Subjects With Refractory Eosinophilic Asthma: a Randomised, Double-blind, Placebo Controlled Trial

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Sep 25, 2015
Registry last updated
Aug 29, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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