drugset / Trial / NCT02156791

Safety, Clinical Tolerability and Immunogenicity of Increasing Doses of gpASIT+TM

NCT02156791 ↗

Phase 2 Completed 61 enrolled BioTech Tools S.A.
NaSingle-groupOpen-labelTreatment

Summary

gpASIT+TM product is based on highly purified allergen fragments obtained from grass pollen. The purpose of this clinical trial is to confirm the safety, clinical tolerability and immunogenicity of increasing doses of gpASIT+TM administered subcutaneously to patients with grass pollen-induced allergic rhinoconjunctivitis, and to determine the maximal tolerated dose of gpASIT+TM .

Timeline

Start
2013-08
Primary completion
2013-12
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject gpASIT+TM Protein / enzyme biologic — Subcutaneous