Found 8 matching trials
Clinical Efficacy and Safety of a Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induced Allergic Rhinoconjunctivitis
PHASE3gpASIT+TM product is based on highly purified allergen fragments obtained f...
Location
University Hospital Ghent
Clinical Efficacy and Safety of Subcutaneous Immunotherapy With gpASIT+™ in Patients With Grass Pollen-induced Allergic Rhinoconjunctivitis
PHASE3This is a randomised, double-blind, placebo-controlled, international, mult...
Location
Multiple Locations
Clinical Safety and Tolerability Study of gpASIT+TM and gpASIT+TM/Immunoregulating Adjuvant to Treat Seasonal Grass Pollen Rhinoconjunctivitis
PHASE1The purpose of this study is to assess the safety and tolerability of gpASI...
Location
UZ Leuven, Gasthuisberg
Safety of gpASIT+TM Subcutaneously Administered to Hay Fever Patients With or Without Immunoregulating Adjuvant
PHASE2The aim of the study is to compare the safety, clinical tolerability, immun...
Location
Universitaire Ziekenhuis van Leuven
Safety and Tolerance Study of Grass Pollen-derived Peptides to Treat Allergic Rhinitis
PHASE1The purpose of this study is to determine whether the oral administration o...
Location
Hospital University Ghent
Safety Study of Grass Pollen-derived Peptides to Treat Seasonal Allergic Rhinoconjunctivitis
PHASE1The purpose of this study is to determine whether the oral administration o...
Location
University Hospital Brugmann
Safety, Clinical Tolerability and Immunogenicity of Increasing Doses of gpASIT+TM
PHASE2gpASIT+TM product is based on highly purified allergen fragments obtained f...
Location
Universitätsklinikum Carl-Gustav-Carus, Dresden, Germany
Clinical Efficacy and Safety of gpASIT+TM to Treat Seasonal Allergic Rhinoconjunctivitis
PHASE2The purpose of the study is to evaluate the efficacy and safety of grass po...
Location
CHR Saint Joseph Warquignies