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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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EUCTR |
Last refreshed on:
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14 March 2016 |
Main ID: |
EUCTR2013-003683-31-PT |
Date of registration:
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04/03/2014 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Long-term safety study of QGE031 in patients with allergic asthma who completed study CQGE031B2201
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Scientific title:
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An open-label, multi-center, extension study to evaluate the long-term safety of subcutaneous 240mg QGE031 given every 4 weeks for 52 weeks in allergic asthma patients who completed study CQGE031B2201 |
Date of first enrolment:
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27/03/2014 |
Target sample size:
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300 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2013-003683-31 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: no
Randomised: no
Open: yes
Single blind: no
Double blind: no
Parallel group: no
Cross over: no
Other: no
If controlled, specify comparator, Other Medicinial Product: no
Placebo: no
Other: no
Number of treatment arms in the trial: 1
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Phase:
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Countries of recruitment
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Argentina
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Canada
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Czech Republic
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Finland
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Germany
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Hungary
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Israel
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Italy
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Korea, Republic of
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Mexico
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Poland
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Portugal
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Romania
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Russian Federation
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Singapore
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Slovakia
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Turkey
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United Kingdom
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United States
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Contacts
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Key inclusion & exclusion criteria
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Inclusion criteria: Key Inclusion Criteria:
- FEV1 > 40% predicted
- patients who completed CQGE031B2201 study
Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 240 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 60
Exclusion criteria: Key Exclusion Criteria:
- life-threatening asthma attack, intubation, respiratory arrest during or after completion of CQGE031B2201 study
- new malignancy
- ongoing SAE from CQGE031B2201 that was assessed as related to study drug
- patient experienced platelets drop to < 75,000/uL
- patient experienced one unexpected grade 4 or two unexpected grade 3 hypersensitivity reactions
- patient is pregnant
Age minimum:
Age maximum:
Gender:
Female: yes Male: yes
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Health Condition(s) or Problem(s) studied
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Asthma MedDRA version: 18.1
Level: PT
Classification code 10003553
Term: Asthma
System Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders
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Therapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]
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Intervention(s)
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Product Code: QGE031 Pharmaceutical Form: Solution for injection
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Primary Outcome(s)
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Secondary Objective:
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Timepoint(s) of evaluation of this end point: Every 4 weeks (as patient visits site every 4 weeks) as described in protocol.
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Main Objective: To assess long-term safety and tolerability of QGE031 given every 4 weeks s.c.
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Primary end point(s): Adverse events and serious adverse events
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Secondary ID(s)
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CQGE031B2201E1
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2013-003683-31-SK
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Source(s) of Monetary Support
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Novartis Pharma Services AG
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Results
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Results available:
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Date Completed:
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