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- W2045292834 abstract "RATIONALE: Omalizumab is a relatively novel therapy approved for treating patients with allergic moderate to severe persistent asthma. It is dosed subcutaneously every 2 - 4 weeks. We examined the efficacy of Omalizumab, in patients who demonstrated significant clinical response, after dosage intervals were extended. This was assessed based upon the proposed half life of IgG being 28 days.METHODS: An IRB approved prospective analysis was performed to assess the efficacy of extended dose intervals of Omalizumab in 31 patients with allergic diseases including persistent asthma, urticaria, angioedema/anaphylaxis, and atopic dermatitis. Quality of life measurements were completed using Juniper Quality of Life measurements.RESULTS: Sixteen female and 15 male patients ranging from 13-80 years old (mean age = 45.1 years), were evaluated in a private practice setting. Their mean IgE level was 779 IU/mL. Of these 31 patients, 29 (94%) demonstrated clinical efficacy after lengthening their dosage interval. 17 of the twenty nine patients started with every 2 weeks dosing, and they were able to extend their Omalizumab dose on average after their ninth dose. 12 of the twenty nine patients started with every 4 weeks dosing, and they were able to extend their Omalizumab dose on average after their eleventh dose.CONCLUSIONS: Extension of dosing intervals of Omalizumab was successful based upon clinical response and maintenance scheduling. This appears likely after the patient's reach steady state concentrations of Omalizumab. Earlier success was noted in those patients who initially received their Omalizumab every two weeks, however lengthening dosage intervals was successful in both groups. RATIONALE: Omalizumab is a relatively novel therapy approved for treating patients with allergic moderate to severe persistent asthma. It is dosed subcutaneously every 2 - 4 weeks. We examined the efficacy of Omalizumab, in patients who demonstrated significant clinical response, after dosage intervals were extended. This was assessed based upon the proposed half life of IgG being 28 days. METHODS: An IRB approved prospective analysis was performed to assess the efficacy of extended dose intervals of Omalizumab in 31 patients with allergic diseases including persistent asthma, urticaria, angioedema/anaphylaxis, and atopic dermatitis. Quality of life measurements were completed using Juniper Quality of Life measurements. RESULTS: Sixteen female and 15 male patients ranging from 13-80 years old (mean age = 45.1 years), were evaluated in a private practice setting. Their mean IgE level was 779 IU/mL. Of these 31 patients, 29 (94%) demonstrated clinical efficacy after lengthening their dosage interval. 17 of the twenty nine patients started with every 2 weeks dosing, and they were able to extend their Omalizumab dose on average after their ninth dose. 12 of the twenty nine patients started with every 4 weeks dosing, and they were able to extend their Omalizumab dose on average after their eleventh dose. CONCLUSIONS: Extension of dosing intervals of Omalizumab was successful based upon clinical response and maintenance scheduling. This appears likely after the patient's reach steady state concentrations of Omalizumab. Earlier success was noted in those patients who initially received their Omalizumab every two weeks, however lengthening dosage intervals was successful in both groups." @default.
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- W2045292834 date "2007-01-01" @default.
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- W2045292834 title "Efficacy of Omalizumab Using Extended Dose Intervals" @default.
- W2045292834 doi "https://doi.org/10.1016/j.jaci.2006.12.199" @default.
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