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Efficacy and Safety Evaluation for the Treatment of Allergy Against Grass and Olive Pollen

Rhinoconjunctivitis Clinical Trial

Official title:
A Randomized, Double-Blinded, Placebo-Controlled, Prospective, Multicenter CT to Evaluate Efficacy and Safety of Subcutaneous Immunotherapy in Subjects With Rhinitis With/Without Mild to Moderate Asthma Sensitized to Olive and Grass Pollen

Clinical Trial Summary

Prospective, multicenter, randomized, double-blind, placebo-controlled clinical trial of efficacy and safety with subcutaneous immunotherapy in patients with mild to moderate rhinitis / rhinoconjunctivitis with or without mild to moderate asthma sensitized to grasses and olive

Clinical Trial Description

Double blind, multicenter, parallel, placebo controlled study. It includes 180 subjects sensitised to olea and grass pollen with mild to moderate rhinitis / rhinoconjunctivitis with or without mild to moderate asthma, from 12 to 65 years of age. Medication treatment during 1 year. The main outcome: CSMS ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04891237
Study type Interventional
Source Inmunotek S.L.
Contact Miguel Casanovas
Phone 912908942
Email mcasanovas@inmunotek.com
Status Recruiting
Phase Phase 3
Start date June 14, 2021
Completion date January 2026
View Details
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