A Study in Patients With Chronic Obstructive Pulmonary Disease
Launched by CHIESI FARMACEUTICI S.P.A. · Nov 19, 2010
Trial Information
Current as of May 27, 2025
Completed
Keywords
ClinConnect Summary
Chronic obstructive pulmonary disease (COPD) is an incurable, debilitating and progressive disease that can be fatal. The recent Global Burden of Disease Study ranks COPD as the 6th leading cause of mortality and the 12th leading cause of morbidity world-wide. Furthermore, trends in the use of medical care resources indicate that the economic cost of COPD continues to rise in direct relation to the ageing population, the increase in prevalence of disease and the cost of new and existing medical and public health interventions.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Male or female patients aged ≥ 40 years, who have signed an Informed Consent form prior to initiation of any study-related procedure or once applicable written informed consent obtained by legal representative.
- 2. Outpatients with a diagnosis of COPD and including:
- • 1. Smoking history of at least 10 pack years defined as \[(number of cigarettes smoked per day) x (number of years of smoking) / 20\], both current and ex-smokers are eligible.
- • 2. Use of bronchodilators in the previous 2 months to visit 1.
- • 3. Post-bronchodilator FEV1 \< 60% of the predicted normal value.
- • 4. Post-bronchodilator FEV1/FVC \< 0.7.
- • 5. A ≥ 5% response to a reversibility test.
- • 6. A Baseline Dyspnoea Index (BDI) focal score less or equal than 10 (to be met also at visit 2).
- • 3. History of no more than one COPD exacerbation in the previous 12 months (without considering the last 2 months) to visit 1.
- • 4. A cooperative attitude and ability to be trained to the proper use of pMDI and DPI (Accuhaler®, circular moulded plastic inhaler) inhalers.
- Main Exclusion Criteria:
- • 1. Clinically relevant respiratory disorders.
- • 2. Current diagnosis of asthma or respiratory disorders other than COPD.
- • 3. Clinically significant laboratory and ECG abnormalities indicating a significant or unstable concomitant disease which may impact the feasibility of the results of the study according to investigator's judgement.
- • 4. Patients with COPD exacerbation in the 2 months prior to screening and during the study period.
- • 5. Patients requiring long term (at least 12 hours daily) oxygen therapy for chronic hypoxemia.
- • 6. Patients treated with depot corticosteroids in the 2 months preceding the visit 1 and during the run-in period.
About Chiesi Farmaceutici S.P.A.
Chiesi Farmaceutici S.p.A. is a global pharmaceutical company headquartered in Parma, Italy, specializing in the research, development, and commercialization of innovative therapeutic solutions. With a strong focus on respiratory diseases, neonatology, and rare diseases, Chiesi is dedicated to improving patient outcomes through advanced science and technology. The company operates in more than 30 countries and invests significantly in R&D to enhance its product portfolio and expand its global reach. Committed to sustainability and social responsibility, Chiesi adheres to the highest ethical standards in clinical trials and strives to address unmet medical needs with cutting-edge therapies.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Rome, , Italy
Patients applied
Trial Officials
Dave Singh, MD
Principal Investigator
The Medicine Evaluation Unit - Manchester, UK
Jorgen Vestbo, MD
Principal Investigator
Dept. of Cardiology and Respiratory Medicine - Copenhagen, Denmark
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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