Omalizumab to Treat Hyper-IgE (Job's) Syndrome
NCT00260702 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 1
Last updated 2017-07-02
Summary
This study will evaluate the safety and effectiveness of a laboratory-made antibody called omalizumab in patients with Job's syndrome, or hyper-IgE syndrome (HIES). Patients with HIES have very high levels of IgE antibody, a protein made by white blood cells. IgE plays an important role in starting allergic reactions in the body and may be related to some HIES symptoms, such as skin rashes and asthma. Patients also have frequent lung infections, easily broken bones and other symptoms. Omalizumab, which is approved to treat allergic asthma, is directed against IgE. This study will see if blocking IgE with omalizumab in HIES patients is safe and if it can reduce patients' IgE count. It will also look at how the body handles omalizumab and how it affects patients' symptoms.
Patients 6 years of age or older with HIES may be eligible for this study. Each candidate is screened with a medical history, physical examination, skin examination and blood test.
Participants receive an injection of omalizumab under the skin once every 2 weeks for 6 doses. At the time of each injection, patients are examined by a doctor, answer questions about their symptoms and have a blood sample drawn. After the sixth dose, patients have a physical examination, blood tests, skin examination and lung function tests. At follow-up visits scheduled 2, 4 and 6 months after the last dose of omalizumab, patients have a physical examination, answer questions about their symptoms, and have a blood sample drawn. Patients who show a significant response to omalizumab stay off the drug for 3 months after the last dose and then discuss with their study doctor and referring doctor about continuing the medicine.
Conditions
- Hyper-IgE Syndrome
- Job's Syndrome
Interventions
- DRUG
-
Omalizumab (Xolair)
Sponsors & Collaborators
-
National Institute of Allergy and Infectious Diseases (NIAID)
lead NIH
Study Design
- Purpose
- TREATMENT
Eligibility
- Min Age
- 6 Years
- Max Age
- 76 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-11-24
- Primary Completion
- 2010-03-19
- Completion
- 2010-03-19
Countries
- United States
Study Locations
More Related Trials
-
The Effect of Xolair ® (Omalizumab) in Mastocytosis Patients
NCT01333293 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Effect of Omalizumab (Xolair) on Basophils in Patients With Chronic Idiopathic Urticaria
NCT01701583 ·Status: COMPLETED ·Phase: PHASE4
-
Treatment of Idiopathic Angioedema With Xolair as Add-on Therapy
NCT02966314 ·Status: COMPLETED ·Phase: PHASE4
-
Study to Evaluate the Therapeutic Equivalence of SYN008 Versus Xolair® in the Treatment of Patients With Refractory Chronic Spontaneous Urticaria
NCT04944602 ·Status: UNKNOWN ·Phase: PHASE3
-
Three-month, Single-center Study to Identify Biomarkers/Response to Xolair Therapy in Chronic Idiopathic Urticaria
NCT02814630 ·Status: COMPLETED ·Phase: NA
-
OIT and Xolair® (Omalizumab) in Cow's Milk Allergy
NCT01157117 ·Status: COMPLETED ·Phase: PHASE2
-
Omalizumab to Treat Eosinophilic Gastroenteritis
NCT00084097 ·Status: COMPLETED ·Phase: PHASE2
-
Peanut Reactivity Reduced by Oral Tolerance in an Anti-IgE Clinical Trial
NCT01781637 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Predicting the Clinical Response to Omalizumab With Anti-Immunoglobulin E (IgE) Ab Response or Syk Expression in Basophils
NCT02023151 ·Status: COMPLETED ·Phase: PHASE4
-
Anti-Interleukin-5 (IL-5) Study for Hypereosinophilic Syndrome
NCT00266565 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Role of Immunoglobulin E (IgE) Bearing Cells in Chronic Idiopathic Urticaria (CIU)
NCT03111628 ·Status: COMPLETED ·Phase: PHASE4
-
Identifying Responders to Xolair (Omalizumab) Using Eosinophilic Esophagitis as a Disease Model
NCT01040598 ·Status: COMPLETED ·Phase: PHASE1
-
The Effects of Omalizumab (Anti-IgE) on the Late-phase Response to Nasal Allergen Challenge
NCT01003301 ·Status: COMPLETED ·Phase: PHASE2
-
Omalizumab in Chronic Spontaneous Urticaria Patients Non Responding to Initial Standard antihistaminE Treatment
NCT02550106 ·Status: COMPLETED ·Phase: PHASE4
-
Xolair in Patients With Chronic Sinusitis
NCT00117611 ·Status: COMPLETED ·Phase: PHASE4
-
The Effect of Omalizumab on Responses to Cat Allergen Challenge
NCT00604786 ·Status: COMPLETED ·Phase: NA
-
Prospective Double-blind Placebo-controlled Study of the Effect of Xolair (Omalizumab) in Chronic Urticaria Patients
NCT01803763 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
A Safety Study of Xolair (Omalizumab) in Patients With Chronic Idiopathic Urticaria (CIU) Who Remain Symptomatic Despite Treatment With H1 Antihistamines, H2 Blockers, and/or Leukotriene Receptor Antagonists
NCT01264939 ·Status: COMPLETED ·Phase: PHASE3
-
A Study About the Use of Omalizumab in the Treatment of Food Allergy and Anaphylaxis
NCT07027163 ·Status: COMPLETED
-
Comparison of Pharmacokinetics and Safety of HS632 and Xolair® With a Single Injection
NCT04361812 ·Status: TERMINATED ·Phase: PHASE1
-
Open-Label Extension Of Intravenous Mepolizumab In Patients With Hypereosinophilic Syndrome
NCT00097370 ·Status: TERMINATED ·Phase: PHASE3
-
E-B-FAHF-2, Multi OIT and Xolair (Omalizumab) for Food Allergy
NCT02879006 ·Status: UNKNOWN ·Phase: PHASE2
-
Study of Efficacy and Safety of Xolair® (Omalizumab) in Chinese Patients With Chronic Spontaneous Urticaria
NCT03328897 ·Status: COMPLETED ·Phase: PHASE3
-
Xolair (Omalizumab) for Treatment of Drug-induced Acute Tubulointerstitial Nephritis (AIN)
NCT01893658 ·Status: WITHDRAWN ·Phase: PHASE2
-
Intravenous Mepolizumab In Subjects With Hypereosinophilic Syndromes (HES)
NCT00086658 ·Status: COMPLETED ·Phase: PHASE3