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Efficacy and Safety/Tolerability of Grass MATA MPL

Study:

Efficacy and Safety/Tolerability of Grass MATA MPL, a Randomized, Placebo-Controlled, Double-Blind Study

Rationale:

n/a

Purpose:

Grass MATA MPL has been developed by Allergy Therapeutics (UK) Ltd. to provide pre-seasonal specific immunotherapy for patients with proven type I hypersensitivity to cross reacting grass pollens causing rhinitis and/or conjunctivitis with or without mild to moderate asthma bronchiale. The purpose of this study is to compare the efficacy of Grass MATA MPL versus placebo in grass-allergic subjects following 4 subcutaneous injections of study medication administered before the start of the 2007 grass pollen season.

Study Status: Completed

Recruiting:
n/a

Condition Intervention Phase
Type I Hypersensitivity Biological: Grass MATA MPL
Biological: Placebo		 Phase 3

Verified by Allergy Therapeutics September, 2009

Sponsored by: Allergy Therapeutics
Information provided by: Allergy Therapeutics
ClinicalTrials.gov identifier: NCT00414141

Study Type: Interventional

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

Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States

Karl Jürgen Fischer von Weikersthal-Drachenberg, MD., Study Chair

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.