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UnknownNCT02879006

E-B-FAHF-2, Multi OIT and Xolair (Omalizumab) for Food Allergy

Double-Blind, Placebo-Controlled Phase 2 Study to Assess Safety and Efficacy of Chinese Herbal Therapy and Multiple Food Allergen Oral Immunotherapy

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
33 (actual)
Sponsor
Xiu-Min Li · Academic / Other
Sex
All
Age
6 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is testing the use E-B-FAHF-2 Chinese herbal therapy in combination with multi-food oral immunotherapy (OIT) and Xolair® (Omalizumab) to help children and adults who are allergic to foods be able to safely tolerate food allergens. Specifically in this protocol, the food allergens are milk, egg, peanut, almond, cashew, hazelnut, walnut, sesame, and/or wheat. Omalizumab is considered an investigational drug for the treatment of food allergies in children and adults. Investigational means it has not been approved by the Food and Drug Administration (FDA) for use in the U.S. The researchers hope to learn whether the addition of Chinese herbal therapy (E-B-FAHF-2) can improve the outcome of sustained unresponsiveness (which is the ability to consume a food allergen and pass an oral food challenge after being off treatment for 3 months) as compared to placebo (i.e. subjects with OIT/Omalizumab + herbal vs. OIT/Omalizumab + placebo), and will help adults and children be able to safely ingest the foods they are allergic to.

Detailed description

Prior studies have shown that this Chinese herbal formulation is safe and well-tolerated in food allergic individuals. While oral immunotherapy (OIT) can lead to desensitization, it remains uncertain whether this treatment can lead to lasting protection. Therefore, this study aims to use the Chinese herbal formula in combination with OIT to determine whether sustained protection can be achieved. All subjects will receive multi-allergen OIT, along with a 4 month course of omalizumab to provide added safety for the initial dose escalation and build up phases. Subjects will be randomized to receive active Chinese herbal formula or placebo. Subjects will be treated with OIT for 2 years and then food challenges will be performed to assess for desensitization. For those who achieve desensitization, all treatments will be discontinued and food challenges will be performed 3 months later to assess for sustained unresponsiveness.

Conditions

Interventions

TypeNameDescription
DRUGChinese Herbal MedicationCapsules, 26 month course, starting 2 months pre-OIT
DRUGPlaceboPlacebo capsules that look identical to E-B-FAHF-2, 26 month course, starting 2 months pre-OIT
DRUGOmalizumab4 months course, starting 2 months pre-OIT through the 2 month build-up phase
DRUGMulti OIT24 months of multi OIT (maintenance dose of 1gm each food allergen)

Timeline

Start date
2016-08-01
Primary completion
2020-11-01
Completion
2020-11-01
First posted
2016-08-25
Last updated
2020-08-12

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02879006. Inclusion in this directory is not an endorsement.