Asthma Clinical Trial
Official title:
Long-Term Study of IGE025 in Moderate to Severe Bronchial Asthma
| Verified date | October 2011 |
| Source | Novartis |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Japan: Ministry of Health, Labor and Welfare |
| Study type | Interventional |
This study will evaluate the safety and efficacy of omalizumab up to 48 weeks in adult
patients with moderate to severe bronchial asthma.
THIS STUDY IS NOT ENROLLING PATIENTS IN THE UNITED STATES
| Status | Completed |
| Enrollment | 133 |
| Est. completion date | March 2006 |
| Est. primary completion date | March 2006 |
| Accepts healthy volunteers | |
| Gender | Both |
| Age group | 20 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - Allergic asthma patients - Inadequately controlled patients Exclusion Criteria: - - History of severe anaphylactoid or anaphylactic reactions - Previous treatment with omalizumab - History of cancer or cancer Other protocol-defined exclusion criteria may apply. |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Japan | This study is not being conducted in the United States | Tokyo |
| Lead Sponsor | Collaborator |
|---|---|
| Novartis | Daiichi Sankyo Co., Ltd. |
Japan,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Safety of omalizumab | |||
| Secondary | Pulmonary function parameters measured by spirometer | |||
| Secondary | Morning and evening peak expiratory flow (PEF) | |||
| Secondary | Symptoms score, treatment score, activities of daily living score, nighttime sleep score, and asthma score |
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