drugset / Trial / NCT02560948

Clinical Efficacy and Safety of a Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induced Allergic Rhinoconjunctivitis

NCT02560948 ↗

Phase 3 Completed 554 enrolled BioTech Tools S.A.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

gpASIT+TM product is based on highly purified allergen fragments obtained from grass pollen. The purpose of this study is to demonstrate the clinical efficacy and safety of a subcutaneous immunotherapy with gpASIT+™ in patients with grass pollen-induced allergic rhinoconjunctivitis compared to placebo.

Timeline

Start
2015-12
Primary completion
2016-08
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject gpASIT+TM Unknown — Subcutaneous