House Dust Mite Allergy Clinical Trial
Official title:
Multicenter Study for Evaluation of Efficacy and Safety of Perennial Specific Immunotherapy With a Depot House Dust Mite Allergen Extract (D. Pteronyssinus 100%) in Patients With House Dust Mite Sensitivity
Verified date | February 2013 |
Source | Allergopharma GmbH & Co. KG |
Contact | n/a |
Is FDA regulated | No |
Health authority | Germany: Paul-Ehrlich-Institut |
Study type | Interventional |
The trial is performed to assess efficacy and safety of Novo-Helisen Depot in allergic Rhinoconjunctivitis
Status | Completed |
Enrollment | 0 |
Est. completion date | February 2006 |
Est. primary completion date | February 2005 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 55 Years |
Eligibility |
Inclusion Criteria: - Positive skin prick test to house dust mite, - Positive RAST test to house dust mite, - Positive provocation test result to house dust mite, Exclusion Criteria: - Serious chronic diseases, - Other perennial allergies |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Germany | Allergopharma GmbH & Co. KG | Reinbek |
Lead Sponsor | Collaborator |
---|---|
Allergopharma GmbH & Co. KG |
Germany,
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