Xolair Enhances Oral Desensitization in Peanut Allergic Patients
This study is ongoing, but not recruiting participants.
Information provided by (Responsible Party):
Dale T Umetsu, Children's Hospital Boston
First received: February 4, 2011
Last updated: January 16, 2013
Last verified: January 2013
This is a pilot feasibility study, using Xolair pretreatment for oral peanut desensitization.
||Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
||Xolair Enhances Oral Desensitization in Peanut Allergic Patients
Primary Outcome Measures:
- ability of a patient to tolerate rapid oral peanut desensitization to a dose of 500 mg peanut (cumulative dose, 1,000 mg). [ Time Frame: First day of desensitization ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
- ability of a patient to tolerate rapid oral peanut desensitization to a dose of 4,000 mg of peanut. [ Time Frame: after 7-8 wks of desensitization ] [ Designated as safety issue: Yes ]
| Estimated Enrollment:
| Study Start Date:
| Estimated Study Completion Date:
| Estimated Primary Completion Date:
||January 2013 (Final data collection date for primary outcome measure)
Experimental: omalizumab, oral desensitization
We hypothesize that pretreatment with anti-IgE mAb will greatly reduce the side effects and allergic reactions that occur during oral desensitization to peanut and will enhance the development of oral tolerance in patients with severe peanut allergy.
|Ages Eligible for Study:
||7 Years to 25 Years
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
- Patients with severe peanut allergy, between the ages of 7-25 years, having a history of significant clinical symptoms within 1 hr of peanut ingestion.
- Total IgE >50 kU/L but <2,0000 kU/L.
- Sensitivity to peanut will be documented by a positive skin prick test result and RAST test to peanut, with 20 kU/L as a lower limit for eligibility.
- Patients must also fail a double blind food challenge with peanut at a dose of 100 mg or less (after a cumulative dose of 186 mg), with minimal or no reactions to the placebo challenge.
- All female subjects of childbearing potential will be required to provide a urine sample for pregnancy testing that must be negative one week before being allowed to participate in the study.
- Subjects must be planning to remain in the study area during the trial.
- Subjects and/or their parents must be trained on the proper use of the Epi-Pen to be allowed to enroll in the study.
Due to the risk of serious systemic anaphylactic reactions to peanut in this study, we will exclude:
- Patients with acute infections, autoimmune disease, severe cardiac disease, and those who are treated with beta-adrenergic antagonistic drugs (beta-blockers, which increase the risk of more serious symptoms of anaphylaxis).
- Subjects having a history of severe anaphylaxis to peanut requiring intubation or admission to an ICU, frequent urticaria, or history consistent with poorly controlled persistent asthma.
- Total IgE > 2,000 IU/mL.
- Subjects with unstable angina, significant arrhythmia, uncontrolled hypertension, chronic sinusitis, or other chronic or immunological diseases that in the mind of the investigator might interfere with the evaluation or administration of the test drug or pose additional risk to the subject e.g. gastrointestinal or gastroesophageal disease, chronic infections, scleroderma, hepatic and gallbladder disease, chronic non-allergic pulmonary disease.
- Subject with an FEV1 or PEF less than 80% predicted with or without controller medication (if able to perform the maneuver) at screening, the oral desensitization visit, or food challenge visit.
- Subjects who have received an experimental drug in the last 30 days prior to admission into this study or who plan to use an experimental drug during the study, who are current users of oral, intramuscular, or intravenous corticosteroids, or tricyclic antidepressants, or who are using medication that could induce adverse gastrointestinal reactions during the study.
- Subjects refusing to sign the EpiPen Training Form.
- Pregnant or breast-feeding females.
- Subjects with severe food associated eczema, dermatitis herpetiformis, eosinophilic esophagitis, eosinophilic enteritis, proctocolitis, food protein induced enterocolitis syndrome (FPIES) or other gastrointestinal diseases. These requirements are necessary to limit the study to patients with primarily IgE mediated peanut allergy, and to exclude patients with peanut sensitivity mediated by cellular/T cell (non-IgE mediated) mechanisms.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01290913
|Children's Hospital Boston, Harvard Medical School
|Boston, Massachusetts, United States, 02115 |
Children's Hospital Boston
||Dale T Umetsu, MD, PhD
||Children's Hospital, Harvard Medical School
||Lynda Schneider, MD
||Children's Hospital, Harvard Medical School
No publications provided
||Dale T Umetsu, Professor, Children's Hospital Boston
History of Changes
|Other Study ID Numbers:
||CHB10090470, Xolair and Peanut Allergy
|Study First Received:
||February 4, 2011
||January 16, 2013
||United States: Food and Drug Administration
Keywords provided by Children's Hospital Boston:
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on October 23, 2014
Immune System Diseases
Respiratory System Agents