drugset / Trial / NCT03211247

Safety and Efficacy Study of Viaskin Peanut in Peanut-allergic Young Children 1-3 Years of Age

NCT03211247 ↗

Phase 3 Completed 414 enrolled DBV Technologies
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study aims to assess the safety and efficacy of Viaskin Peanut to induce desensitization to peanut in peanut-allergic children 1 to 3 years of age after a 12-month treatment by EPicutaneous ImmunoTherapy (EPIT).

Timeline

Start
2017-07-31
Primary completion
2019-08-20
Completion
2022-04-27

Outcome

Met primary endpoint

registry analysis (other test); Part B Viaskin Peanut 250 mcg vs Part B Placebo; p <0.001; Proportion difference 33.4 (95% CI 22.36 to 44.49); Wald test NCT03211247 ↗

release “The FDA confirmed that the Company’s Phase 3 EPITOPE study met the pre-specified criteria for success for the primary endpoint.” dbv-technologies.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Viaskin Peanut Protein / enzyme biologic 100 ug Other
Subject Viaskin Peanut Protein / enzyme biologic 250 ug Other

Indications