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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT01032304
Other study ID # ERD-01-08/EP
Secondary ID
Status Unknown status
Phase Phase 3
First received December 11, 2009
Last updated June 12, 2014
Start date August 2009
Est. completion date September 2015

Study information

Verified date June 2014
Source Edmond Pharma
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to evaluate the effect of erdosteine, compared to placebo, on exacerbation rate over a 12-month treatment period in patients with moderate-to-severe COPD. Moreover, the effects of erdosteine on pulmonary function parameters, clinical symptoms and quality of life, and the long-term safety of the drug will be assessed.


Recruitment information / eligibility

Status Unknown status
Enrollment 492
Est. completion date September 2015
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- COPD stage II-III GOLD

- At least 2 exacerbations in the previous 2-12 months

Exclusion Criteria:

- Acute exacerbations in the 2 months prior to enrolment

- Diagnosis of asthma and/or other relevant lung diseases

- COPD stage IV

- Unstable concurrent diseases

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Erdosteine
One 300 mg capsule twice a day
Placebo
One capsule twice a day

Locations

Country Name City State
Belgium Campus Gasthuisberg Dep.t Longfunctiemetingen Leuven
Bulgaria ASMOH-MC "Sveti Panteleiomon" Sofia
Bulgaria Clinic for emergency Medicine and Intensive care, Pneumology and Physiatry Sofia
Bulgaria Clinic of Pulmonary Disease-Military Medical Academy Sofia
Bulgaria Clinical of Pneumology and Physiatry Varna
Czech Republic Plicnì Ordinace Havlìckuv Brod
Czech Republic Poliklinica Moravsky Krumlov Moravsky Krumlov
Czech Republic Department of Respiratory Medicine, Faculty Hospital Olomouc
Czech Republic Lerymed spol. s.r.o. Praha
Czech Republic Lipa Centrum Nove Butovice Praha
Czech Republic Plicnì M.I.O., spol. s.r.o. Pribor
Czech Republic Plicnì Ambulance Prostejov
Czech Republic Plicnì Ordinace Strakonice
Czech Republic Nemonice Znojmo Znojmo
Denmark Department of Respiratory Diseases, Copenhagen University Hospital Hvidovre
France Service de Pneumologie, Hopital Bichat Paris
France Service de Pneumologie, Hopital Bois-Guillaume Rouen
Italy Dip. Pneumologia Osp. G. Rummo Benevento
Italy U.O. Pneumologia Bussolengo
Italy UOC di Pneumologia- Ospedale Civile di Massa e Carrara Carrara
Italy UOC Pneumologia Riabilitativa INRCA Casatenovo Lecco
Italy Ospedale Careggi, Malattie dell'Apparato Respiratorio Firenze
Italy UOC Pneumologia Osp. Vito Fazzi Lecce
Italy UOC di Pneumologia-Ospedale Mater Salutis Legnago Verona
Italy U.O. Pneumologia Macerata
Italy Ospedale San Carlo Borromeo, Dipartimento Broncocardiopneumologico Milano
Italy UO di Pneumologia Osp. San Paolo Milano
Poland Szpital Uniwersytecki 2 Bydgoszczy
Poland Klinika Pulmonologii II Katedry, Collegium Medicum Uniwersytetu Krakow
Poland Katedra Pulmunologii i Alergologii, Klinika Gruzlicy Uniwersytetu Medycznego Lodz
Poland Katedra i klinika Pulmonologii, Uniwersytet Medyczny Poznan
Poland NZOZ "Darmeticus" Warsawa
Poland Katedra i Klinika Pneumonologii, Warszawski Uniwersytet Medyczny Warszawa
Romania Institutul de Pneumoftiziologie "Marius Nasta" Bucharest
Romania Novo Medica Bucharest
Romania Spitalul de Pneumoftiziologie "Leon Daniello" Cluj
Romania Spitalul Clinic de Pneumoftiziologie Iasi
Romania Clinica Pneumologie I, Spitalul Clinic Judetean Mures Targu Mures
Romania Spitalul de Pneumoftiziologie "Victor Babes" Timisoara
Slovakia Nemocnica s Poliklinicou "Svateho Jakuba"n.o. Bardejov
Slovakia Inspiro Humenne
Slovakia Specializovana NemocnicaSvorada Zobor n.o. Nitra
Slovakia Narodny Ustav Tuberculozy Vysne Hagy
United Kingdom Regional Respiratory Centre, Belfast City Hospital Belfast
United Kingdom Cardiovascular and Respiratory Studies Department Hull
United Kingdom Aintree Chest Centre, University Hospital Aintree Liverpool

Sponsors (1)

Lead Sponsor Collaborator
Edmond Pharma

Countries where clinical trial is conducted

Belgium,  Bulgaria,  Czech Republic,  Denmark,  France,  Italy,  Poland,  Romania,  Slovakia,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of acute exacerbations 12 months
Secondary spirometry parameters 12 months
Secondary COPD symptoms 12 months
Secondary Quality of life 12 months
Secondary Safety and tolerability of erdosteine 12 months
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