Allergic Asthma Clinical Trial
Official title:
Predicting the Clinical Response to Omalizumab With Anti-IgE Response or Syk Expression in Basophils
This research is being done to test whether differences in blood cells at baseline (start of the study) can be used to predict how well omalizumab will work in a patient. Omalizumab (Xolair) is a drug approved by the U.S. Food and Drug Administration (FDA) to treat asthma. Studies show that omalizumab improves the symptoms of asthma but some people experience better improvement than others.
From a therapeutic perspective, the study will determine whether changes in the peripheral
blood basophil response to crosslinking anti-IgE Ab during treatment with omalizumab predicts
the clinical efficacy of treatment with the drug. Secondary outcomes measures would focus on
whether the starting level of anti-IgE-mediated histamine release, or the changes syk
expression or its starting level would be sufficient to predict the clinical outcome.
The study is a single-site trial to evaluate the utility of baseline basophil measures to
predict the efficacy of subcutaneously administered omalizumab as an add-on therapy for the
treatment of adult patients 18−75 years old who have been diagnosed with moderate to severe
asthma according to current approved guidelines. Patients will be treated with omalizumab
according to the standard FDA approved dosing table for a period of 16 weeks.
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