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Completed

NCT Number: NCT00314574

A Study of Omalizumab (Xolair) in Subjects With Moderate to Severe Persistent Asthma (EXTRA)

This is a multicenter, randomized, double-blind, placebo-controlled study of the efficacy, safety, and tolerability of subcutaneously administered Xolair as add-on therapy for the treatment of subjects aged 12-75 years old diagnosed with moderate to severe asthma who are inadequately controlled with high-dose inhaled corticosteroids (ICS)+ long-acting beta-agonists (LABA) with or without additional controller therapy.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed Informed Consent Form and an informed assent, if applicable
  • Be between the ages of 12 to 75 years
  • Have had a history of moderate to severe asthma for at least one year prior to screening
  • Have had treatment with a stable regimen of of salmeterol 50 µg twice a day (BID) or formoterol 12 µg BID for at least 8 weeks prior to screening
  • Have had treatment with a stable regimen of high-dose inhaled corticosteroids (ICS) for at least 8 weeks prior to screening
  • Have inadequately controlled asthma
  • Have had at least one asthma exacerbation requiring systemic corticosteroid rescue in the 12 months prior to the screening visit while receiving treatment with high-dose ICS
  • Have less than 10 pack-years smoking history
  • Have a positive skin test for or a positive, in vitro response to one relevant perennial aeroallergen documented within the 12 months prior to screening
  • If a subject has not had a positive skin test or in vitro reactivity in the 12 months prior to screening, the subject must demonstrate a positive response to at least one relevant perennial aeroallergen in a skin or in vitro test prior to randomization
  • Female subjects of childbearing potential must use an effective method of contraception from screening through their duration of participation in the study
  • For the collection of additional blood samples for future research (optional), provide signed consent and an informed assent, if applicable.

Exclusion criteria

  • Have had an asthma exacerbation requiring intubation within 12 months prior to screening
  • Have active lung disease other than asthma
  • Have had an asthma exacerbation requiring treatment with the addition of systemic (oral or intravenous) corticosteroids or an increase in systemic corticosteroids within 30 days prior to screening
  • Require chronic immunosuppressive therapy including cyclosporine, methotrexate, etc.
  • Have significant medical illness other than asthma
  • Have taken methotrexate, gold salts, cyclosporine, or macrolide antibiotics, within 3 months prior to screening
  • Have taken other investigational drugs within 30 days prior to screening
  • Have been treated with Xolair within the 12 months prior to screening
  • Have a history of drug or alcohol abuse that, in the judgment of the investigator, may put the subject at risk for being unable to participate fully in the study for the duration of the study
  • Have elevated serum IgE levels for reasons other than allergy
  • Are pregnant or lactating

Treatment and study plan

Omalizumab (Xolair)

Drug

Omalizumab (Xolair) was administered by subcutaneous (SC) injection every 2 or 4 weeks. Xolair was supplied as a sterile, white, preservative-free, lyophilized powder in single-use vials that were reconstituted with Sterile Water for Injection (SWFI), USP.

Other names: Xolair

Placebo

Drug

Placebo was administered by subcutaneous (SC) injection every 2 or 4 weeks. Placebo contained the same ingredients as the lyophilized formulation of Xolair,excluding omalizumab.

Corticosteroids

Drug

Minimum dose of 500 µg of fluticasone dry-powder inhaler or its equivalent ex-valve dose twice a day.

long-acting beta-agonists

Drug

50 µg salmeterol twice daily or 12 µg formoterol twice daily.

Primary outcomes

  1. Rate of Asthma Exacerbations Over the 48 Week Treatment Period

    Time frame: 48 weeks

    A protocol-defined asthma exacerbation was defined as worsening of asthma symptoms requiring treatment with systemic corticosteroids for 3 or more days; for patients receiving long-term oral corticosteroids, an exacerbation was a 20 mg or more increase in average daily dose of oral prednisone (or a similar dose of another systemic corticosteroid). The rate of protocol-defined asthma exacerbations, normalized by subject-time at risk and computed over the 48 week treatment period in each treatment group.

Secondary outcomes

  1. Change From Baseline in Total Asthma Symptom Scores

    Time frame: Baseline and Week 48

    Change from baseline to week 48 in Total Asthma Symptom Score (TASS), which included a nocturnal asthma score (0 to 4 scale), morning asthma symptoms (yes or no), and a daytime asthma symptom score (0 to 4 scale, total score range 0 to 9, higher TASS scores represent worse symptoms; breathlessness, tightness in chest, wheezing and cough. Score achieved by week 48 minus baseline.

  2. Change From Baseline in the Number of Puffs Per Day of Beta Agonist Rescue Medication

    Time frame: Baseline and Week 48

    Change from baseline to week 48 in mean puffs per day of albuterol. Puffs per day was achieved by week 48 minus baseline.

  3. Change From Baseline in Overall Asthma-related Quality of Life

    Time frame: Baseline and Week 48

    Change from baseline to week 48 in overall asthma-specific health-related quality of life, as measured by the standardized version of the Asthma Quality of Life Questionnaire (AQLQ[S]) score. The AQLQ(S) consists of 4 domains (activity limitations, symptoms, emotional function, and environmental stimuli), with a total of 32 items; the overall score is the mean of these 32 items on a scale of 1 to 7 (1 = severe impairment, 7 = no impairment). Overall outcome achieved by mean visit minus baseline.

  4. Number of Participants Assessed for Frequency and Severity of Treatment-emergent Adverse Events

    Time frame: Week 48

    This outcome is represented in the adverse event section of the database.

Sponsors and collaborators

Lead sponsor

Genentech, Inc.

Industry

Registry information

Official study title

A Phase IIIb Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of Xolair in Subjects With Moderate to Severe Persistent Asthma Who Are Inadequately Controlled With High-Dose Inhaled Corticosteroids and Long-Acting Beta-Agonists

Important dates

Study start
2005
Primary completion
2009
Study completion
2009
First posted
Apr 14, 2006
Registry last updated
Feb 9, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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