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Efficacy and Safety Evaluation for the Treatment of Allergy Against Mites — MM09-SIT-023  

Rhinoconjunctivitis Clinical Trial

Official title:
Randomized, Double-blinded, Placebo-controlled, Prospective, Multicenter Trial to Evaluate the Efficacy and Safety of SIC in Subjects With Mild/Moderate Asthma and Rhinitis/Rhinoconjunctivitis Sensitized to D.Pteronyssinus and/or D. Farinae

Clinical Trial Summary

A double-blinded, placebo-controlled, prospective, multicenter randomized of 2 active treatment groups, compared to 1 placebo group, for the determination of the efficacy and safety of subcutaneous immunotherapy in patients with rhinitis/rhinoconjunctivitis with mild to moderate asthma, sensitised to Dermatophagoides pteronyssinus and /or Dermatophagoides farinae.

Clinical Trial Description

Double blind, multicenter, parallel placebo controlled study. It includes 150 subjects sensitised to mites, from 14 to 65 years of age. Medication treatment of 1 year. The main outcome: CSMS ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04435990
Study type Interventional
Source Inmunotek S.L.
Contact Francisco Moreno, MD
Phone 956292100
Email dr.moreno@drlobaton.org
Status Recruiting
Phase Phase 3
Start date October 6, 2020
Completion date December 2025
View Details
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