Status:
COMPLETED
Omalizumab in Patients With Moderate to Severe Persistent Allergic Asthma Not Adequately Controlled Despite GINA (2009) Step 4 Therapy
Lead Sponsor:
Novartis Pharmaceuticals
Collaborating Sponsors:
Genentech, Inc.
Conditions:
Persistent Allergic Asthma
Eligibility:
All Genders
18-75 years
Phase:
PHASE3
Brief Summary
This study will assess the efficacy, safety and tolerability of omalizumab, compared to placebo in 18 to 75 year old Chinese patients with moderate to severe persistent allergic asthma who have inadeq...
Eligibility Criteria
Inclusion
- Met study drug-dosing table eligibility criteria (serum baseline total IgE level ≥ 30 to ≤ 700 IU/mL and body weight \> 20 kg and ≤ 150 kg)
- Diagnosed with asthma ≥ 1 year duration at Screening, and a history of asthma that is not adequately controlled with GINA (2009) Step 4 therapy
- Received medium-to-high dose inhaled corticosteroid \> 500 µg Beclomethasone Diproprionate (BDP), or equivalent plus regularly inhaled LABA, either separately or in combination, for at least 8 weeks prior to screening
- Met specific asthma exacerbations eligibility criteria prior to the screening period
- Exhibited inadequate symptom control as demonstrated by specific criteria (in keeping with GINA 2009 guidelines)
- Positive skin prick test to at least one perennial aeroallergen documented by a historical test within 12 months prior to screening, or at Visit 1
- FEV1 ≥ 40% and \< 80% of the predicted normal value for the patient (using local standards), after withholding bronchodilators at Visit 2
Exclusion
- Used other investigational drugs at the time of enrollment, or within 30 days or 5 half-lives of enrollment, whichever is longer. For biological agent-based investigational drugs, such as monoclonal antibodies, at least six months will need to have passed between the last administration of the drug and the patient's Screening Visit.
- History of malignancy
- History of allergies and diseases that could interfere with the analyses
- Clinically significant abnormality on a 12-lead ECG recorded at Visit 1
- Elevated IgE levels for reasons other than allergy
- Current smokers, or a former smoker with a smoking history of \> 10 pack-years. A former smoker must have abstained for a minimum of 12 months before randomization
- Receiving specific medications
- Clinically significant laboratory abnormalities (not associated with the study indication) at Visit 1
- Other protocol-defined inclusion/exclusion criteria may apply
Key Trial Info
Start Date :
September 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2013
Estimated Enrollment :
616 Patients enrolled
Trial Details
Trial ID
NCT01202903
Start Date
September 1 2010
End Date
October 1 2013
Last Update
March 23 2015
Active Locations (39)
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1
Novartis Investigative Site
Beijing, Beijing Municipality, China, 100023
2
Novartis Investigative Site
Beijing, Beijing Municipality, China
3
Novartis Investigative Site
Guangzhou, Guangdong, China, 510030
4
Novartis Investigative Site
Guangzhou, Guangdong, China, 510515