Status:

COMPLETED

Efficacy and Safety From a High-dosed Sublingual Grass Pollen Preparation

Lead Sponsor:

Allergopharma GmbH & Co. KG

Conditions:

Allergy

Rhinitis

Eligibility:

All Genders

18-65 years

Phase:

PHASE3

Brief Summary

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

Eligibility Criteria

Inclusion

  • Allergic rhinoconjunctivitis attributable to grass pollen
  • Positive SPT
  • Positive EAST
  • Positive provocation Test

Exclusion

  • Serious chronic disease
  • other perennial allergies

Key Trial Info

Start Date :

March 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2012

Estimated Enrollment :

126 Patients enrolled

Trial Details

Trial ID

NCT00623701

Start Date

March 1 2008

End Date

October 1 2012

Last Update

November 8 2013

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Prof. Kristian Reich, MD

Hamburg, Germany, 20354

Efficacy and Safety From a High-dosed Sublingual Grass Pollen Preparation | DecenTrialz