drugset / Trial / NCT01538979

Phase II Study of Grass Pollen Allergy Vaccine BM32

NCT01538979 ↗

Phase 2 Completed 181 enrolled Biomay AG
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study will evaluate the efficacy and safety of BM32 in grass pollen allergic subjects. It will test the hypothesis that either of two doses of BM32 will lead to a sustained relief off allergy symptoms over a two year study period.

Timeline

Start
2012-03
Primary completion
2014-12
Completion
2015-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BM32 Vaccine 20 ug Subcutaneous
Subject BM32 Vaccine 40 ug Subcutaneous