drugset / Trial / NCT01720251

Efficacy Study of a Preseasonal Treatment With AllerT in Subjects With Birch Pollen Allergy

NCT01720251

Phase 2 Completed 240 enrolled Anergis
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The main objective of the trial is to demonstrate the efficacy of a two months pre-seasonal treatment with AllerT 100 µg maintenance dose in reducing symptoms of allergic rhinoconjunctivitis during the following birch pollen season

Timeline

Start
2012-10
Primary completion
2013-09
Completion
2013-09

Drugs

EvaluationDrugModalityDoseRoute
Subject AllerT Peptide 50 ug Subcutaneous
Subject AllerT Peptide 100 ug Subcutaneous

Indications