Omalizumab for the Treatment of Food Allergy in Patients With Elevated Total IgE Levels

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

In this project, the investigators would like to learn if 24 weeks (about 5 and a half months) of omalizumab injections, given every 2 weeks, will be safe and effective for food allergic people who have a total immunoglobulin E (IgE) above the current FDA approved dosing regimen enabling a person to increase tolerance to the food(s) that the person is allergic to. The investigators would also like to learn if participants who demonstrate increased tolerance to food after 24 weeks of omalizumab, can introduce the food into the diet utilizing an additional 8 weeks (about 2 months) of twice weekly omalizumab injections.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Maximum Age: 55
Healthy Volunteers: f
View:

• Age 1 to 55 years

• A positive prick skin test (PST) with a wheal ≥ 6 mm to at least one of the relevant foods (peanut, cashew, walnut, egg, milk, or wheat)

• Positive food-specific IgE (≥2.0 kilo units of allergen-specific IgE per liter (kUA/L)) to at least one of the study specific foods

• A weight / IgE level that would have excluded the participant from the OUTMATCH study based on the dosing table noted above

• Positive double-blind, placebo-controlled food challenge (DBPCFC) to one of the relevant foods at a cumulative dose of ≤144 mg (maximum tolerated dose ≤30 mg)

Locations
United States
Maryland
Johns Hopkins
RECRUITING
Baltimore
Contact Information
Primary
Robert Wood, MD
rwood@jhmi.edu
410-955-5883
Time Frame
Start Date: 2025-05-19
Estimated Completion Date: 2027-10-15
Participants
Target number of participants: 32
Treatments
Other: Treatment with omalizumab
This is an open label study of omalizumab with no placebo. Participants who meet study inclusion criteria and are enrolled in the study will receive omalizumab. The dose of omalizumab will be based on participant's weight.
Related Therapeutic Areas
Sponsors
Collaborators: Genentech, Inc.
Leads: Johns Hopkins University

This content was sourced from clinicaltrials.gov