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Clinical Trial Summary

Prospective, randomized, placebo-controlled, multicenter of 3 active treatment groups, compared to 1 placebo group, for the determination of the efficacy and safety of subcutaneous immunotherapy in patients with mild to moderate asthma and allergic rhinitis/rhinoconjunctivitis (intermittent or persistent) due to hypersensitivity to house dust mites (Dermatophagoides pteronyssinus and / or D. farinae) and grass pollen


Clinical Trial Description

Double blind, parallel placebo-controlled study. The subjects will receive medication during 11 months ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04874714
Study type Interventional
Source Inmunotek S.L.
Contact
Status Terminated
Phase Phase 3
Start date April 30, 2021
Completion date October 9, 2023

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