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Sponsored by: |
Allergopharma Joachim Ganzer KG |
Information provided by: | Allergopharma Joachim Ganzer KG |
ClinicalTrials.gov Identifier: | NCT00264459 |
The trial is performed to asses efficacy and safety of a sublingual extract of a six grass pollen mixture
Condition | Intervention | Phase |
Grass Pollen Allergy |
Biological: Grass pollen formulation |
Phase III |
MedlinePlus related topics: | Allergy Hay Fever |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | A Multicentre, Placebo-Controlled, Double-Blind Study to Evaluate Efficacy and Safety of a Perennial Sublingual Specific Immunotherapy With a Liquid Formulation of an Extract of a Six Grass Pollen-Mixture in Patients With Clinically Relevant Grass Pollen Sensitivity. |
Ages Eligible for Study: | 18 Years to 60 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Rhinitis, Rhinoconjunctivitis, Positive Rast result to grass pollen, Positive skin prick test to grass pollen, Positive specific provocation to grass pollen,
Exclusion Criteria:
Serious chronic diseases, Other perennial allergies
Leader in specific allergy research and therapy 
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Study ID Numbers: | Al0102st |
First Received: | December 12, 2005 |
Last Updated: | July 24, 2008 |
ClinicalTrials.gov Identifier: | NCT00264459 |
Health Authority: | Germany: Paul-Ehrlich-Institut |
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