drugset / Trial / NCT02223182
Efficacy and Safety of Viaskin Milk in Children With IgE-Mediated Cow's Milk Allergy
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |