Subcutaneous Immunotherapy in Patients Sensitized to Phleum Pratense

Status Completed

Clinical Trial Summary

Based on EMA (European Medicines Agency) new guidelines on the clinical development of products for immunotherapy for the treatment of allergic disease the aim of this study was to assess safety and tolerability of three different subcutaneous immunotherapy dose escalations in patients allergic to the pollen of Phleum pratense.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01489033
Study type	Interventional
Source	Roxall Medicina España S.A
Contact
Status	Completed
Phase	Phase 1
Start date	January 2010
Completion date	May 2010

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