NL-OMON45129
Completed
Phase 2
A phase IIa, randomized, double-blind, placebo controlled, parallel group study to assess the safety and efficacy of subcutaneously administered BI 655066 (risankizumab) as add-on therapy over 24 weeks in patients with severe persistent asthma. - 1311.14
Overview
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Boehringer Ingelheim
- Enrollment
- 3
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 to 99 (—)
Inclusion Criteria
- •1\. Male or female patients aged at least 18 years but not more than 75 years.
- •2\. Pre\-bronchodilator clinic measured FEV1 of \>\=40% and \<\=85% of predicted normal at the screening visit.
- •3\. A minimum of one year history of asthma diagnosed by a physician, and have FEV1 reversibility as defined by an improvement in FEV1 \>\=12% and an absolute change of at least 200 ml starting within 15 to 30 minutes after administration of 400 µg salbutamol (albuterol) via MDI. Reversibility testing is performed at the screening visit (visit 1B). If reversibility criteria are not met, the patient may still be randomized if there is:
- •\- documented evidence of reversibility with improvement in FEV1 \>\=12% above baseline and an absolute increase of at least 200 ml in the 2 years prior to visit 2 (randomization visit) or
- •\- documented evidence of airway hyperresponsiveness (methacholine: PC20 of \<8 mg/ml) in the 2 years prior to visit 2 (randomization visit) or
- •\- documented evidence of airflow variability in clinic FEV1 \>\=20% between two clinic visits documented in the 12 months prior to visit 2 (randomization visit)
- •If reversibility criteria are not met at visit 1B and if any of the above historic data are not available, reversibility testing can be repeated up to twice during screening period at seperate visits. For the first retest, 400 µg salbutamol via MDI should be used, and for the second retest, up to 800 µg salbutamol via MDI or 2\.5 mg nebulized albuterol should be used. Reversibility testing must not occur on the day of randomization. Additional guidelines for reversibility testing can be found in Appendix 10\.1\.
- •4\. Patients must be on at least medium dose inhaled corticosteroids and at least one other asthma controller medication for at least one year prior to the date of screening. Asthma therapy must have been documented and must be stable for at least 4 weeks prior to the date of screening.
- •5\. Patients must have documented history of at least one of the following criteria:
- •a) two or more severe asthma exacerbations in the last 12 months, or
Exclusion Criteria
- •1\. Patients with a significant disease other than asthma.
- •2\. Patients who are not able to produce sputum or sputum samples of sufficient quality.
- •3\. Patients who had clinically relevant history of intubation for asthma exacerbation in the past year.
- •4\. Patients diagnosed with any concurrent respiratory disease.
- •5\. Recent history (within 6 months) of myocardial infarction or hospitalized for cardiac failure in the past year.
- •6\. Patients who have undergone thoracotomy with pulmonary resection.
- •7\. Patients who have undergone bronchial thermoplasty or radiotherapy procedure in the past year or have planned procedures during the study.
- •8\. Patients taking oral corticosteroids with a total daily dose of more than 20 mg prednisone (or equivalent) in the past 6 weeks.
- •9\. Pregnant or nursing women.
- •10\. Women of childbearing potential that, if sexually active, is unwilling to use a highly effective method of birth control.
Investigators
Similar Trials
Active, not recruiting
Phase 1
Efficacy and safety of BI 655066/ABBV-066 (risankizumab) in patients with severe persistent asthma.Severe AsthmaTherapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]EUCTR2014-004932-20-PLBoehringer Ingelheim RCV GmbH & CoKG200
Active, not recruiting
Phase 1
Efficacy and safety of BI 655066 in patients with severe persistent asthmaEUCTR2014-004932-20-ITBOEHRINGER-INGELHEIM ITALIA S.P.A.369
Active, not recruiting
Phase 1
Efficacy and safety of BI 655066 (risankizumab) in patients with severe persistent asthma.EUCTR2014-004932-20-GBBoehringer Ingelheim Limited200
Active, not recruiting
Not Applicable
Efficacy and safety of BI 655066 in patients with severe persistent asthma.Severe AsthmaTherapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]EUCTR2014-004932-20-HUBoehringer Ingelheim RCV GmbH & CoKG450
Active, not recruiting
Phase 1
Efficacy and safety of BI 655066 (risankizumab) in patients with severe persistent asthma.EUCTR2014-004932-20-BESCS Boehringer Ingelheim Comm.V200