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Evaluation of the Efficacy and Safety of MV130 in Chronic Obstructive Pulmonary Disease (COPD) — MV130  

Chronic Obstructive Pulmonary Disease (COPD) Clinical Trial

Official title:
Randomized Double-blind Placebo-controlled Prospective, Parallel, Multicentre Clinical Trial of Bacterial Vaccine Administered by Sublingual Mucosa in Subjects With COPD for Efficacy and Safety Evaluation and Immunomodulatory Response

Clinical Trial Summary

The purpose of the study is to evaluate the efficacy and safety of a biological vaccine (MV130 in subjects with Chronic Obstructive Pulmonary Disease (COPD) compared with a placebo group.

Clinical Trial Description

Double blind parallel placebo controlled study. The subjects will receive medication during 12 months and will be followed up during another six months ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01842360
Study type Interventional
Source Inmunotek S.L.
Contact
Status Active, not recruiting
Phase Phase 2/Phase 3
Start date April 2013
Completion date March 2023
View Details
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