| January 11, 2008 |
| April 16, 2008 |
| January 2008 |
| April 2008 (final data collection date for primary outcome measure) |
| Subjects will have QOL measures (RSDI, SNOT 20, SF-36), NPIF, and nasal lavage repeated. Exacerbations of sinusitis requiring additional treatments will be recorded. Paranasal sinus CT scans will be obtained at the screening and final visits [ Time Frame: At entry and every 4 weeks ] [ Designated as safety issue: No ] |
| Same as current |
| Complete list of historical versions of study NCT00603785 on ClinicalTrials.gov Archive Site |
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| Effects of Anti-IgE Antibody Omalizumab on Patients With Chronic Sinusitis |
| Effects of Anti-IgE Antibody Omalizumab (Xolair) on Patients With Chronic Sinusitis and a Positive Allergen Test |
We propose to study the effects of Xolair on patients with chronic sinusitis with or without nasal polyps. Because of the similarities between the inflammatory processes found in asthmas and rhinitis to those found in chronic sinusitis, we hypothesize that sinusitis should respond to Xolair, just as asthma. |
We propose to study the effects of Xolair on patients with chronic sinusitis with or without nasal polyps. Since Xolair has been shown to be effective in asthmatic subjects with evidence of atopy and elevated IgE, we will limit our study to patients with chronic sinusitis and these parameters. The primary objective is to determine if Xolair decreases mucosal thickness on CT scan after 6 months of treatment. |
| Phase IV |
| Interventional |
| Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Efficacy Study |
| Chronic Sinusitis |
- Drug: Placebo
- Drug: Xolair
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- Placebo Comparator: Subjects to receive placebo treatment for 6 months
- Experimental: Subjects to receive Xolair treatment for 6 months
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| Withdrawn |
| 25 |
| April 2008 |
| April 2008 (final data collection date for primary outcome measure) |
Inclusion Criteria:
- Males and females between 18 and 75 years of age
- Chronic sinusitis as defined by symptoms for greater than 12 weeks despite treatment.
- Paranasal sinus CT scan showing evidence of chronic sinusitis.
- Positive skin or RAST test to an inhalant allergen.
- Serum total IgE between 30 and 700 International Units/ml.
- Body weight less than 150kg.
- Impaired quality of life as measured by the Rhinosinusitis Disability Index (RSDI).
Exclusion Criteria:
- Women of childbearing potential not using the contraception method(s) (Birth control pills, depo Provera, double barrier) as well as women who are breastfeeding.
- Known sensitivity to Xolair
- Patients with severe medical conditions that in the view of the investigator prohibits participation in the study (heart, lung, kidney, neurological, oncologic or liver disease).
- Use of any other investigational agent in the last 30 days.
- No measurable disability on the RSDI.
- Immunocompromised patients or patients with ciliary disorders.
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| Both |
| 18 Years to 75 Years |
| No |
| Contact information is only displayed when the study is recruiting subjects |
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| NCT00603785 |
| Andrew Goldberg, MD, University of California, San Francisco |
| 07030836, BB-IND# 12452 |
| University of California, San Francisco |
| University of Chicago |
| Principal Investigator: |
Andrew Goldberg, MD |
University of California, San Francisco |
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| University of California, San Francisco |
| April 2008 |