A Study to Measure Serum Periostin, Asthma-Related Biomarkers and Response to Prednisolone in Adult and Adolescent Patients With Severe Oral Corticosteroid-Dependent Asthma

Exclusion Criteria

• •Baseline FEV1 \</=39% of predicted
• •Asthma exacerbation (as defined by protocol) within 28 days before the time of informed consent or during Screening
• •Major episode of infection requiring admission to hospital for \>/=24 hours or treatment with intravenous antibiotics within the 28 days before the time of informed consent or during Screening or requiring treatment with oral antibiotics within the 14 days before the time of informed consent or during Screening
• •Active parasitic infection or Listeria monocytogenes infection within the 6 months before the time of informed consent
• •For adults active tuberculosis (TB) requiring treatment within the 12 months before the time of informed consent (patients are also required to have no recurrence of symptoms in the 12 months following completion of TB treatment), or for adolescents history of active TB requiring treatment
• •Known history of severe clinically significant immunodeficiency
• •Evidence of acute or chronic hepatitis or known liver cirrhosis
• •Inadequate liver function
• •Diagnosis or history of malignancy, or current investigation for possible malignancy
• •Other clinically significant medical disease that is uncontrolled despite treatment or that is likely, in the opinion of the investigator, to require a change in therapy or affect the ability to participate in the study
• •Current smoker or former smoker with a smoking history of \>15 pack-years
• •Current use of an immunomodulatory/immunosuppressive therapy or past use within three months or five drug half-lives (whichever is longer) before the time of informed consent
• •Use of a biologic therapy (including omalizumab) at any time during the 4 months before the time of informed consent
• •History of anaphylaxis with omalizumab treatment or history of anaphylaxis to any therapeutic biological agent
• •Use of zileuton or roflumilast at any time during the two months before the time of informed consent
• •Initiation of or change in allergen immunotherapy within three months before the time of informed consent
• •Treatment with an investigational agent within 30 days of informed consent or 5 half-lives of the investigational agent, whichever is longer
• •Pregnant or lactating women
• •Body mass index (BMI) \>38 kg/m2
• •Body weight \<40 kg