![]() Clinical Trials - Colorado
Contact for all studies: 1) Mild to Moderate Asthma Study Clinical Trial Description: We are studying an experimental nutritional drink for the treatment of asthma in children. The purpose of this study is to determine whether this nutritional drink can increase asthma free days by assessing the frequency of daily asthma symptoms in children with mild to moderate persistent asthma. Dr. Stanley Szefler, Principal Investigator / Kelli Brown-Engelhardt, Study Coordinator To be eligible you must be: Qualified participants may receive physical examinations, ECG's, lung function tests, skin testing and study drug at no cost. In addition, participants who qualify to participate in the study will be financially compensated. 2) Moderate to Severe Uncontrolled Allergic Asthma Study Clinical Trial Description: This study is designed to demonstrate one-year efficacy and safety data for subcutaneous (SQ) Xolair®, compared to placebo in children 6 to <12 years with moderate to severe persistent asthma, who have inadequate asthma control despite treatment with medium to high dose inhaled corticosteroids. Dr. Henry Milgrom, Principal Investigator / Kelli Brown-Engelhardt, Study Coordinator To be eligible you must be: Qualified participants may receive physical examinations, ECG's, lung function tests, skin testing and study drug at no cost. In addition, participants who qualify to participate in the study will be financially compensated. 3) Peanut Allergy Study Clinical Trial Description: Peanut allergy is the most common food allergy in the United States, affecting 1.5 million people. We are currently conducting a research study that is investigating the efficacy of Xolair® in reducing the risk of peanut-induced allergic reactions. Xolair is designed to bind to the IgE in the body and lower the risk of allergic reactions. IgE is a protein that has been shown to play an important part in allergic reaction. This study will test your reaction to peanuts after 24 weeks of treatment with Xolair or placebo (a substance that contains no medication). Dr. Donald Leung, Principal Investigator / Amanda Calhoun, Study Coordinator To be eligible you must be: Duration: 38 weeks participation in study with approximately 16 visits to the clinic. Qualified participants may receive physical examinations, ECG's, lung function tests, skin testing, and study drug at no cost. In addition, participants who qualify to participate in the study will be financially compensated.
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