Regulatory Lymphocytes in Patients Treated With Specific Immunotherapy

PHASE4CompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

March 31, 2007

Primary Completion Date

October 31, 2010

Study Completion Date

December 31, 2010

Conditions
ImmunotherapySeasonal Allergic Rhinitis
Interventions
DRUG

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.

OTHER

placebo

placebo administered with the same scheme and doses as specific subcutaneous immunotherapy

Trial Locations (1)

90-153

Department of Pneumonology and Allergy, Medical University of Lodz, Lodz

All Listed Sponsors
lead

Ministry of Science and Higher Education, Poland

OTHER_GOV

NCT01475188 - Regulatory Lymphocytes in Patients Treated With Specific Immunotherapy | Biotech Hunter | Biotech Hunter