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A Phase III Trial Investigating the Efficacy and Safety of Grazax in Children Aged 5-16 Years With Grass Pollen Induced Rhinoconjunctivitis With or Without Asthma

NCT00408616 Phase 3 COMPLETED

The purpose of this study is to investigate if immunotherapy with Grazax is safe and reduces the hayfever symptoms and the use of symptom relieving medications in children during the grass pollen season

Details

Lead sponsorALK-Abelló A/S
PhasePhase 3
StatusCOMPLETED
Enrolment253
Start date2006-11
Completion2007-11

Conditions

Interventions

Primary outcomes

Countries

Germany