Treatment of Adult Allergic Asthma Patients with MEMP1972A
- Conditions
- Allergic AsthmaMedDRA version: 14.1Level: PTClassification code 10003553Term: AsthmaSystem Organ Class: 10038738 - Respiratory, thoracic and mediastinal disordersTherapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]
- Registration Number
- EUCTR2011-003997-10-HU
- Lead Sponsor
- GENENTECH, Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 560
- Age 18-75 years
- Body weight = 40 kg
- Normal CXR
- Diagnosis of asthma for at least 12 months
- Evidence of documented bronchodilator reversibility
- Prebronchodilator FEV1 = 40% and = 80% predicted
- Daily use of ICS and second controller for a minimum of 3 consecutive months prior to screen
- History of at least one protocol-defined asthma exacerbation in the 18 months prior to screen
- Inadequately controlled asthma despite compliance with asthma controller therapy documented by daily diary and ACQ
- Positive aeroallergen-specific IgE OR a total serum IgE = 75 IU/mL
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 540
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 20
- Asthma exacerbation requiring systemic steroids in the 30 days prior to randomization
- Have pre-existing active lung disease other than asthma
- Any infection including chronic or latent infections or infections requiring treatment during screening
- Clinically significant medical disease that is uncontrolled despite treatment
- Any condition that contraindicates the use of an investigational drug
- History of significant exposure to water-borne parasites and/or have recent diarrheal illness of indeterminate etiology
- Former smoker with >10 pack year history or current smoker
- History of anaphylaxis or allergic reaction during the use of a monoclonal antibody
- Use of any excluded concomitant therapies
- Men and women who are not willing to use highly effective method of contraception
- Women who are pregnant or lactating
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method