drugset / Trial / NCT02851277

A Study to Evaluate Safety, Tolerability and Immune Response in Adults Allergic to Peanut After Receiving Intradermal or Intramuscular Administration of ASP0892 (ARA-LAMP-vax), a Single Multivalent Peanut (Ara h1, h2, h3) Lysosomal Associated Membrane Protein DNA Plasmid Vaccine

NCT02851277 ↗

Phase 1 Completed 31 enrolled Astellas Pharma Global Development, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety and tolerability of ASP0892 after intradermal or intramuscular injection in adults with peanut allergy.

Timeline

Start
2016-12-13
Primary completion
2018-12-06
Completion
2018-12-06

Drugs

EvaluationDrugModalityDoseRoute
Subject ASP0892 Vaccine 1 mg Intramuscular
Subject ASP0892 Vaccine 4 mg Intramuscular

Indications