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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
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 sponsor | ALK-Abelló A/S |
|---|---|
| Phase | Phase 3 |
| Status | COMPLETED |
| Enrolment | 253 |
| Start date | 2006-11 |
| Completion | 2007-11 |
Conditions
- Allergy
Interventions
- Grazax-R
- Grazax Placebo
Primary outcomes
- Hayfever symptoms — Grass pollen season 2007
- Intake of hayfever symptom relieving medication — Grass pollen season 2007
Countries
Germany