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The Safety and Efficacy of a Peanut Immunotherapy Dissolving Film for Peanut Allergy

Peanut Allergy Clinical Trial

Official title:
The Safety and Efficacy of a Peanut Immunotherapy Dissolving Film for Peanut Allergy

Clinical Trial Summary

The purpose of this study is to determine if a new method of administration of peanut sublingual immunotherapy, a dissolving peanut film, is effective.

Clinical Trial Description

Peanut allergy is a common problem with no current treatment. Recent studies have shown some success with oral or sublingual immunotherapy for the treatment of food allergy. Oral treatment, which requires very high doses, is associated with a small but appreciable risk of systemic reactions. Sublingual immunotherapy, which utilizes much smaller doses, is safer but constraints inherent in the available methods of sublingual administration have limited the utility of this method. Typically sublingual immunotherapy for food allergy has used either fresh foods or a simple liquid extract. These methods are not optimized for practicality or dwell duration in the mouth, and, thus far, dosing has been limited by the ability to make concentrated extracts and by the volume of extract that can be applied to the sublingual space. This study is being conducted to determine if a dissolving peanut extract film, will improve efficacy for immunotherapy for peanut allergy. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01897077
Study type Interventional
Source Johns Hopkins University
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date November 2012
Completion date February 3, 2013
View Details
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