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Efficacy and Safety of Subcutaneous Immunotherapy in Birch Pollen Allergic Patients

Allergy Clinical Trial

Official title:
Double-Blind Placebo-Controlled Study of Subcutaneous Immunotherapy in Birch Pollen Allergic Patients

Clinical Trial Summary

To compare versus placebo the efficacy and safety of recombinant Bet v1, natural purified Bet v1 and birch pollen licenced extract used for subcutaneous immunotherapy.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00410930
Study type Interventional
Source Stallergenes
Contact
Status Terminated
Phase Phase 2
Start date November 2002
Completion date November 2005
View Details
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