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Quality of Life in Daxas-treated Patients Older Than 18 Years With Severe COPD (DINO)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Severe COPD

Treatments

Drug: Daxas

Study type

Observational

Funder types

Industry

Identifiers

NCT01285180
U1111-1136-8860 (Registry Identifier)
RO-2455-402-DE

Details and patient eligibility

About

Daxas (roflumilast) is the first oral anti-inflammatory phosphodiesterase inhibitor (PDE-4) for patients with severe chronic obstructive pulmonary disease (COPD) experiencing chronic cough and sputum and with a history of exacerbations as add-on to bronchodilator treatment. With its mode of action Daxas can reduce exacerbations rates and improve lung function parameters which may result in a better health-related quality of life and an improved long-term management of COPD.

The aim of this non-interventional study is to evaluate data on quality of life in COPD patients in Germany in a real life medical setting. Evaluation is based on two COPD specific questionnaires to assess the patient's health status over six months. During the study, socio-demographic data and cost-of-illness data will be recorded. Daxas (tablet) will be administered once daily. The study will provide further data on the safety and tolerability of Daxas.

Enrollment

5,472 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Main Inclusion Criteria:

  • severe COPD

Main Exclusion Criteria:

  • Child pugh (classified B and C)

Trial design

5,472 participants in 1 patient group

DINO
Treatment:
Drug: Daxas

Trial contacts and locations

2412

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Data sourced from clinicaltrials.gov

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