Efficacy and Safety of Roflumilast Taken in the Morning or Evening in Patients With Stable Asthma (12 to 70 y) (BY217/M2-015)

NCT00163475 | Completed Phase 3

• 1 other identifier: BY217/M2-015
• Study Type: interventional
• Target: 511
• Locations: 5 countries
• Sites: 5

Brief Summary

Bronchial asthma is among the world's most prevalent diseases. Roflumilast is a novel, orally active, selective enzyme inhibitor (phosphodiesterase 4 inhibitor), which has shown effectiveness in the treatment of asthma. The aim of the study is to compare the effect of roflumilast on lung function, symptoms, and use of rescue medication in patients with stable asthma. Roflumilast will be administered orally either in the morning or in the evening at one dose level. The study duration consists of a baseline period (1 to 2 weeks) and a treatment period (6 weeks). The study will provide further data on safety, tolerability, and effectiveness of roflumilast.

Conditions

Asthma

Keywords

Asthma; Roflumilast

Outcome Measures

Primary Outcomes (1)

• mean change from randomization to endpoint in forced expiratory volume in one second.

Secondary Outcomes (6)

• forced expiratory vital capacity

• peak expiratory flow

• morning and evening peak expiratory flow (patient's diary)

• symptom score and use of rescue medication (patient's diary)

• Asthma Control Questionnaire (ACQ)

Interventions

Roflumilast DRUG

Eligibility Criteria

• Age: 12 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Written informed consent
• Diagnosis of persistent bronchial asthma (with reference to the Global Initiative for Asthma Guidelines 2002)
• Baseline FEV1 50 - 85% in patients either untreated or receiving e.g. short-acting bronchodilators, DSCG, nedocromil, anticholinergics, long-acting bronchodilators, theophylline/aminophylline, lipoxygenase inhibitors, leukotriene antagonists, alone or in combination
• Baseline FEV1 60 - 90% in patients receiving not more than 500 mcg BDP-CFC (or equivalent) and/or in combination with any other asthma medication mentioned above
• No change in the asthma treatment 4 weeks prior to baseline period
• Patients who, with the exception of asthma, are in good health

You may not qualify if:

• Poorly controlled asthma: requirement of a course of oral and/or parenteral glucocorticosteroids 4 weeks prior to the baseline, or admission to hospital for asthma (including treatment in an emergency room) 4 weeks prior to the baseline period, or asthma exacerbation in the last 4 weeks prior to baseline period
• Patient using regularly \>8 puffs/day rescue medication prior to baseline
• History of lower airway infection in the last 4 weeks prior to baseline period
• Diagnosis of chronic obstructive pulmonary disease and/or other relevant lung diseases
• Heavy smoker: currently: \>20 cigarettes/day and/or \>10 pack years, ex-smoker: with a smoking history of ≥10 pack years
• Clinically relevant abnormal laboratory values suggesting an unknown disease and requiring further clinical evaluation
• Liver insufficiency (Child Pugh A or worse)
• Active hepatitis
• Known infection with HIV
• Diagnosis or history of cancer (other than basal cell carcinoma) or recurrence within 5 years prior to study start
• Alcohol and/or drug abuse
• Suspected hypersensitivity and/or contraindication to any ingredients of the study medication (roflumilast) or rescue medication
• Pregnancy or patient of childbearing potential who is not using reliable method of contraception
• Patients not able to follow study procedures, e.g. due to language problems, psychological disorders
• Suspected inability or unwillingness to comply with the study procedures

Sponsors & Collaborators

• AstraZeneca: lead

Study Sites (5)

ALTANA Pharma

Cities in Australia, Australia

Location

ALTANA Pharma

Cities in Belgium, Belgium

Location

ALTANA Pharma

Cities in France, France

Location

ALTANA Pharma

Cities in South Africa, South Africa

Location

ALTANA Pharma

Cities in Spain, Spain

Location

Related Publications (1)

• Bateman ED, Bousquet J, Aubier M, Bredenbroker D, O'Byrne PM. Roflumilast for asthma: Efficacy findings in non-placebo-controlled comparator and dosing studies. Pulm Pharmacol Ther. 2015 Dec;35 Suppl:S11-9. doi: 10.1016/j.pupt.2015.10.002. Epub 2015 Oct 8.

  PMID: 26456372 DERIVED

Related Links

• BY217-M2-015-RDS-2006-06-09

MeSH Terms

Conditions

Asthma

Interventions

Roflumilast

Condition Hierarchy (Ancestors)

Bronchial Diseases; Respiratory Tract Diseases; Lung Diseases, Obstructive; Lung Diseases; Respiratory Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases

Study Officials

• AstraZeneca AstraZeneca

  AstraZeneca

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 12, 2005
• First Posted: September 14, 2005
• Study Start: May 1, 2004
• Primary Completion: August 1, 2005
• Study Completion: August 1, 2005
• Last Updated: October 25, 2016

Record last verified: 2016-09

Locations

ES (1); FR (1); BE (1); AU (1); ZA (1)