NCT Number: NCT00073177
Efficacy and Safety of Roflumilast in Patients With Asthma (BY217/M2-012)
The aim of the study is to compare the effects of oral roflumilast with placebo on lung function in patients with asthma.
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Notify MeKey information
Conditions
Age range
18 year–70 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
ALTANA Pharma, Cities in Argentina, Argentina
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
- Persistent bronchial asthma
- No change in asthma treatment within 4 weeks prior to visit 1
- Non-smoker or ex-smoker (for 12 months or longer)
Main Exclusion Criteria:
- Poorly controlled asthma or seasonal asthma
- History of lower airway infection four weeks prior to visit 1
- Chronic obstructive pulmonary disease (COPD) and/or other relevant lung disease
- Patients using > 8-puffs/day-short-acting bronchodilator (beta-agonists) (more than 3 days per week on average) prior to visit 1
- Clinically relevant abnormal laboratory values suggesting an undiagnosed disease, severe renal insufficiency, active hepatitis or an HIV infection
- Diagnosis, treatment or remission of any cancer (other than basal cell carcinoma) within two years prior to visit 1
- Patients with chronic heart failure
- Suspected hypersensitivity and/or contraindication to roflumilast or albuterol/salbutamol
- Female patients of childbearing potential not using adequate means of birth control or pregnant or breast-feeding females
- Patients who have received any investigational medication or device in the month prior to visit 1 or who plan to use another investigational medication during the study
Treatment and study plan
Primary outcomes
-
change in lung function from baseline to final visit.
Secondary outcomes
-
pulmonary function variables
-
diary variables
-
quality of life variables
-
time to first exacerbation
-
number of asthma exacerbations
-
safety.
Sponsors and collaborators
Lead sponsor
AstraZeneca
Industry
Registry information
Official study title
A 24 Week, Double-Blind, Randomized, Placebo-Controlled Clinical Trial to Evaluate the Efficacy and Safety of Oral Roflumilast (250 mcg or 500 mcg) Daily in Patients With Asthma
Important dates
- Study start
- 2003
- First posted
- Nov 19, 2003
- Registry last updated
- Oct 25, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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