CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 1 enrolled
Drug / intervention
Omalizumab (Xolair)drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00260702
NCT00260702Phase 1Completed

Pilot Study of Omalizumab (Xolair) in Hyper IgE (Job's) Syndrome

National Institute of Allergy and Infectious Diseases (NIAID)·interventional·Posted Dec 1, 2005·Updated Jul 2, 2017

In Brief

A Phase 1 clinical trial evaluating Omalizumab (Xolair) for Hyper-IgE Syndrome and Job's Syndrome. Completed, enrolled 1 participant across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedDec 1, 2005
Enrollment StartNov 24, 2005
Primary CompletionMar 19, 2010
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 20.6 years ago

Interventions

Omalizumab (Xolair)drug