drugset / Trial / NCT01682070

SUBLIVAC FIX Phleum Pratense DT/DRF

NCT01682070 ↗

Phase 2 Completed 266 enrolled HAL Allergy
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The aim of the study is to determine the optimal effective dose of SUBLIVAC FIX Phleum pratense based on reduction of upper airways reactivity after 5 months of treatment with different dosages of SUBLIVAC FIX Phleum pratense compared to placebo. Furthermore, safety and tolerability will be assessed by the number of related Adverse Events of different dosages of SUBLIVAC FIX Phleum pratense compared to placebo.

Timeline

Start
2012-09
Primary completion
2013-05
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Subject SUBLIVAC FIX Phleum Prat. Unknown 3333 unknown —
Subject SUBLIVAC FIX Phleum Prat. Unknown 10000 unknown —
Subject SUBLIVAC FIX Phleum Prat. Unknown 20000 unknown —
Subject SUBLIVAC FIX Phleum Prat. Unknown 40000 unknown —

Indications