41
Participants
Start Date
March 31, 2007
Primary Completion Date
October 31, 2010
Study Completion Date
December 31, 2010
Allergovit
commercially available grass pollen allergoid (100%), concentration A (1000 TU/ml, therapeutic units/ml)concentration B (10000 TU/ml).Patients were given subcutaneous injections with initial dose of 0.1 ml (concentration A) was increased once a 7 (+7) days until the highest tolerated dose (0.6, concentration B) was reached and SIT was continued with injections once every 4 - 6 weeks up to two years.
placebo
placebo administered with the same scheme and doses as specific subcutaneous immunotherapy
Department of Pneumonology and Allergy, Medical University of Lodz, Lodz
Ministry of Science and Higher Education, Poland
OTHER_GOV