Clinical Trials Directory

Trials / Completed

CompletedNCT00492076

Efficacy and Safety Trial of Subcutaneous Immunotherapy in Mite Induced Asthma

A Randomised, Double-Blind Placebo-Controlled Study Assessing the Short-Term Effect of a Dermatophagoides Pteronyssinus Extract, Quantified in Mass Units, in Subjects With Perennial Mite Induced Asthma

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
45 (actual)
Sponsor
ALK-Abelló A/S · Industry
Sex
All
Age
14 Years – 55 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether a short course of subcutaneous immunotherapy is efficacious in mite induced asthma. The efficacy is based on reduction in control medication.

Detailed description

The control of mild-moderate persistent asthma include the need of concomitant medication, as inhaled corticosteroids. However, compliance in perennial asthma is low. The aim of this study is to assess the possibility to reduce the need of concomitant medication through a short-course of subcutaneous immunotherapy.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPangramin Plus D. pteronyssinus 100%1. Active. Pangramin Plus D. pteronyssinus 100% 2. Placebo. Pangramin Plus placebo

Timeline

Start date
2006-10-01
Primary completion
2008-05-01
Completion
2008-05-01
First posted
2007-06-27
Last updated
2008-10-16

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT00492076. Inclusion in this directory is not an endorsement.