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Multicenter Trial of Immunotherapy With House Dust Mite Allergoid

Phase 3
Completed
Conditions
Rhinoconjunctivitis
Registration Number
NCT00540631
Lead Sponsor
Allergopharma GmbH & Co. KG
Brief Summary

Multicenter Immunotherapy House Dust Mite Allergoid

Detailed Description

A multicentre randomized placebo-controlled double-blind clinical trial for evaluation of safety and efficacy of a specific immunotherapy with an aluminium hydroxide-adsorbed allergoid preparation of house dust mite (Dermatophagoides pteronyssinus) in patients with rhinitis/rhinoconjunctivitis and/or allergic asthma bronchiale

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
108
Inclusion Criteria
  • Positive SPT
  • Positive EAST
  • Positive specific provocation test
Exclusion Criteria
  • Serious chronic diseases
  • other perennial allergies

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
The primary endpoint is the change of the area under the curve (AUC)of the Symptom-Medication-Score (SMS)after 2 years of double-blind treatment to baselineNovember 2007 - February 2010
Secondary Outcome Measures
NameTimeMethod
Change of the AUC of the SMS after one year to baseline.1 year
Change of Nasal Eosinophil Cationic Protein (ECP) after 2 years to baseline2 years
Immunologic changes IgE, IgG1 and IgG42 years
Tolerability and safety of treatments during the entire study period4 years

Trial Locations

Locations (1)

Allergopharma GmbH & Co. KG

🇩🇪

Reinbek, Germany

Allergopharma GmbH & Co. KG
🇩🇪Reinbek, Germany

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