drugset / Trial / NCT02223182

Efficacy and Safety of Viaskin Milk in Children With IgE-Mediated Cow's Milk Allergy

NCT02223182 ↗

Phase 1/2 Completed 198 enrolled DBV Technologies
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objectives of this study are to evaluate the safety and efficacy of Viaskin Milk after 12 months of epicutaneous immunotherapy (EPIT) treatment, for desensitizing IgE-mediated cow's milk allergic children and to assess the long-term safety and therapeutic benefit with Viaskin Milk.

Timeline

Start
2014-11
Primary completion
2017-12-14
Completion
2020-12-22

Outcome

Missed primary endpoint

paper 24 of 49 responders (49.0%) overall vs 16 of 53 responders (30.2%) in the placebo group (odds ratio, 2.19; 95% CI, 0.91-5.41; P = .09) PMID 38407859 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Viaskin Milk Protein / enzyme biologic 150 ug Other
Subject Viaskin Milk Protein / enzyme biologic 300 ug Other
Subject Viaskin Milk Protein / enzyme biologic 500 ug Other

Indications