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Clinical Trial Summary

Efficacy and Safety from a high-dosed sublingual grass pollen preparation


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00623701
Study type Interventional
Source Allergopharma GmbH & Co. KG
Contact
Status Completed
Phase Phase 3
Start date March 2008
Completion date October 2012

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