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Omalizumab Use and Asthma-Related Quality of Life in Patients With Severe Persistent Allergic Asthma

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This study investigates asthma-related quality of life in Brazilian patients using omalizumab.

Official Title

A Randomised, Open-Label, Multicenter Study to Evaluate the Effect of Xolair (Omalizumab) as Add-on Therapy to Inhaled Corticosteroid + Long-Acting Beta Agonist in Fixed or Flexible Dosing Compared to Isolated Inhaled Corticosteroid + Long-Acting Beta Agonist in Fixed or Flexible Dosing in the Asthma-Related Quality of Life in Patients With Severe Persistent Allergic Asthma.

Conditions

  • Asthma

Study Type

Interventional

Study Design

Treatment, Randomised, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study.

Further Details

Primary Outcome Measures:

  • Patient’s quality of life assessed by Asthma Quality of Life Questionnaire score

Secondary Outcome Measures: 

  • Episodes of asthma exacerbation during 5 months of treatment
  • Efficacy assessed by asthma exacerbation data, patient diary cards, rescue medication use, clinical symptoms scores, global evaluations, and pulmonary function.
  • Safety assessed by adverse

Study Start

November 2007

Eligibility & Criteria

  • Ages Eligible for Study: 12 Years to 75 Years
  • Genders Eligible for Study: Both
  • Accepts Healthy Volunteers: No

Inclusion Criteria:

  • 12 to 75 years-old during screening visit.
  • Body weight > 20 kg and < 150kg.
  • Daily or persistent asthma symptoms.
  • Night symptoms at least once a week.
  • Forced Expiratory Volume in 1 second (FEV1) > 40% and < 80% of predicted normal value and continuing asthma symptoms.
  • FEV1 increased > 12% from baseline within 30 minutes of inhaled (up to 400 mcg) or nebulised (up to 5 mg) salbutamol.
  • Subject taking more than 500mcg/day of fluticasone or equivalent associated to a long-acting β2-agonist.
  • Inhaled corticosteroid and LABA doses must remain fixed during the last 04 weeks prior to visit 2.
  • Medical history of at least two episodes of asthma exacerbation treated with systemic corticoid or at least one severe asthma exacerbation treated with systemic corticoid and hospitalisation or emergence room visit in the last 12 months prior to screening visit.
  • Positive skin prick test (diameter of wheal > 3mm) to at least one perennial aeroallergen (dust mite, cat/dog dander, cockroaches), to which the subject is likely to be exposed during the study.
  • Subject capable to read and understand Asthma Related quality of life questionnaire (Juniper’s questionnaire).

Exclusion Criteria:

  • Pregnant, nursing female subjects.
  • Female subjects without current acceptable contraceptive method.
  • Previous history of allergy or hypersensitivity to Omalizumab.
  • Subjects with prior treatment with Omalizumab.
  • Subjects with medical history of psychiatric disorder.
  • Subject has been treated with systemic corticosteroid for any reason other than asthma.
  • Subject took β2 antagonist medication in the last 3 months prior to screening visit.
  • Subject took protocol prohibited medication prior to screening
  • Medical history of food or drug related severe anaphylactoid reactions.
  • Medical history of antibiotics allergy. Patients may be included if the antibiotics to which they are allergic to will be avoided for the entire duration of the study.
  • Asthma related to non-steroidal anti-inflammatory drug (NSAID).
  • Treatment of exacerbation in the 4 weeks prior to randomisation.
  • Other active lung diseases.
  • Medical history of others uncontrolled diseases 3 months prior randomisation (e.g. infections, coronary heart diseases and metabolic diseases).
  • Any history of cancer.
  • Abnormal electrocardiogram (ECG), laboratory exams (clinically significant abnormalities) and chest X-ray (CXR).
  • Evidence or history of drug or alcohol abuse.
  • Airway infection (e.g. pneumonia, acute sinusitis) 4 weeks prior to screening visit
  • Smokers or smoking history of > 10 pack-years.
  • Subject that has been treated with investigational drugs over the past 30 days or during the course of the trial.
  • Subject with elevated IgE levels for reasons other than allergy.
  • Other protocol-defined inclusion/exclusion criteria may apply.

Total Enrolment

123

Contact Details

Please refer to this study by its ClinicalTrials.gov identifier: NCT00567476

Contacts

Novartis
41 61 324 1111      

Locations

Novartis Investigator Site
São Paulo, Brazil    

Sponsors and Collaborators

Novartis

Investigators

Study Chair:      

Novartis Pharma 
Novartis

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Dates

Posted On: 1 January, 2013
Modified On: 16 September, 2014

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