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Keep this study
Lead
Novartis
Age
40–80
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Male and/or female subjects from 40-80 years (inclusive) of age
Subjects have a clinical diagnosis of COPD
Smokers or Ex-smokers with a smoking history of at least 20 pack years
Post-bronchodilator forced expiratory volume in 1 second (FEV1 ) at screening ≤ 50% of the predicted normal value
Post-bronchodilator FEV1/FVC ratio \< 70%
History of at least one treated exacerbation during the 24 months year prior to screening or C-Reactive Protein (CRP) ≥3.47 mg/L,
Subjects should have no concomitant other lung disease or significant concomitant medical conditions that would affect the subjects' safety when participating in the study, or that would be expected to impact on the results of the study
Female subjects must have been surgically sterilized at least 6 months prior to screening or must be using two forms of contraception, or postmenopausal women
Able to provide written informed consent prior to study participation.
Able to communicate well with the investigator and comply with the requirements of the study.
You may not be if
COPD exacerbation(s) requiring treatment within 4 weeks prior to first dosing
History of lung reduction surgery
Any undiagnosed nodule on chest x-ray
Presence of certain medical conditions as specified by the protocol
Subjects requiring oral or parenteral corticosteroids equivalent to \> 10 mg/day or \> 20 mg every other day of prednisone or prednisolone
Participation in any clinical investigation within 4 weeks prior to dosing or longer if required by local regulation.
Donation or loss of 400 mL or more of blood within 8 weeks prior to dosing.
A past medical history of clinically significant electrocardiogram (ECG) abnormalities or a family history of a prolonged QT-interval syndrome.
A known hypersensitivity to drugs similar to the study drug.
History of immunocompromise, including a positive HIV test result.
A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result.
History of drug or alcohol abuse within the 12 months prior to screening or evidence of such abuse as indicated by the laboratory assays conducted during screening.
Clareo Health | Safety and Efficacy of Multiple Doses of Canakinumab (ACZ885) in Chronic Obstructive Pulmonary Disease (COPD) Patients