drugset / Trial / NCT03094845

Safety and Clinical Tolerability of hdmASIT+TM Peptides Administered in HDM-induced Allergic Patients

NCT03094845 ↗

Phase 2 Completed 36 enrolled ASIT Biotech S.A.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

hdmASIT+TM product is based on highly purified allergen fragments from house dust mites. The purpose of this study is to assess the safety and clinical tolerability of subcutaneous immunotherapy with hdmASIT+TM in patients with house dust mite-induced allergic rhinoconjunctivitis compared to placebo.

Timeline

Start
2016-09-28
Primary completion
2017-01-12
Completion
2017-01-23

Drugs

EvaluationDrugModalityDoseRoute
Subject hdmASIT+TM Unknown — Subcutaneous