search
Back to results

Efficacy and Safety of Oral Roflumilast Taken With Low Dose Inhaled Corticosteroids in Patients With Asthma (12 to 70 y) (BY217/M2-013)

Primary Purpose

Asthma

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Roflumilast
Sponsored by
AstraZeneca
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring Asthma, Roflumilast, Corticosteroids

Eligibility Criteria

12 Years - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Main Inclusion Criteria: Written informed consent Diagnosis of persistent chronic bronchial asthma, according to Global Initiative for Asthma (GINA) guidelines The patient has been receiving BDP - CFC ≤1000 mcg per day or equivalent for the previous four weeks FEV1 between 60 and 90% predicted at visit 1 No change in asthma treatment within 4 weeks prior to visit 1 Main Exclusion Criteria: Patients with poorly controlled asthma defined as requiring a course of oral or parenteral corticosteroids, admission to hospital for asthma (including treatment in an emergency room), or exacerbation of asthma in the four weeks prior to visit 1 Patients who suffer from seasonal asthma alone or patients who are likely to have a major exacerbation of their asthma due to seasonal effects during the study run-in or treatment period A history of lower airway infection in the four weeks prior to visit 1 A diagnosis of chronic obstructive pulmonary disease (COPD) and/or other relevant lung disease (e.g. cystic fibrosis, bronchiectasis) Heavy smoker currently smoking >20 cigarettes per day and/or >10 pack years or the patient is an ex-smoker who has smoked >10 pack years Patients using >8 puffs/day relief medication regularly prior to visit 1 Clinically relevant abnormal laboratory values suggesting an unknown disease and requiring further clinical evaluation A diagnosis, treatment or remission of any cancer (other than basal cell carcinoma) within two years prior to visit 1 Patients with chronic heart failure class III or IV (New York Heart Association) Suspected hypersensitivity and/or contraindication to any ingredients of the study medication (roflumilast, BDP, or salbutamol) A history of alcoholism or substance abuse within the 12 months prior to visit 1 Pregnancy or women of childbearing potential who are not using a reliable method of contraception

Sites / Locations

  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma
  • ALTANA Pharma

Outcomes

Primary Outcome Measures

change in forced expiratory volume in 1 second from baseline to final visit.

Secondary Outcome Measures

change from baseline to each visit for spirometry variables, forced vital capacity, mean expiratory flow, peak expiratory flow
change from baseline to each visit based on diary data variables (asthma symptom scores: daytime, nighttime, and summary, use of rescue medication, diurnal variability)
number of rescue free/symptom free days based on the diary card
area under the curves over the full 24-week trial period for the diary variables
number of exacerbations
time to first exacerbation
change from baseline according to the Asthma Quality of Life Questionnaire (AQLQ).

Full Information

First Posted
September 12, 2005
Last Updated
December 1, 2016
Sponsor
AstraZeneca
Collaborators
Pfizer
search

1. Study Identification

Unique Protocol Identification Number
NCT00163527
Brief Title
Efficacy and Safety of Oral Roflumilast Taken With Low Dose Inhaled Corticosteroids in Patients With Asthma (12 to 70 y) (BY217/M2-013)
Official Title
A 24-Week, Double-Blind, Parallel Group, Placebo and Active Controlled Study to Investigate the Efficacy and Safety of Daily Oral Roflumilast Taken With Low Dose Inhaled Corticosteroids in Patients With Chronic Asthma
Study Type
Interventional

2. Study Status

Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
April 2003 (undefined)
Primary Completion Date
November 2005 (Actual)
Study Completion Date
November 2005 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AstraZeneca
Collaborators
Pfizer

4. Oversight

5. Study Description

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 investigate the effect of roflumilast taken orally together with low dose inhaled corticosteroids on lung function. Roflumilast will be administered at one dose level once daily together with inhaled corticosteroids at one dose level twice daily. The study duration consists of a baseline period (2 to 6 weeks) and a treatment period (24 weeks). The study will provide further data on safety, tolerability, and effectiveness of roflumilast.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Asthma, Roflumilast, Corticosteroids

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
2054 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Roflumilast
Primary Outcome Measure Information:
Title
change in forced expiratory volume in 1 second from baseline to final visit.
Secondary Outcome Measure Information:
Title
change from baseline to each visit for spirometry variables, forced vital capacity, mean expiratory flow, peak expiratory flow
Title
change from baseline to each visit based on diary data variables (asthma symptom scores: daytime, nighttime, and summary, use of rescue medication, diurnal variability)
Title
number of rescue free/symptom free days based on the diary card
Title
area under the curves over the full 24-week trial period for the diary variables
Title
number of exacerbations
Title
time to first exacerbation
Title
change from baseline according to the Asthma Quality of Life Questionnaire (AQLQ).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Main Inclusion Criteria: Written informed consent Diagnosis of persistent chronic bronchial asthma, according to Global Initiative for Asthma (GINA) guidelines The patient has been receiving BDP - CFC ≤1000 mcg per day or equivalent for the previous four weeks FEV1 between 60 and 90% predicted at visit 1 No change in asthma treatment within 4 weeks prior to visit 1 Main Exclusion Criteria: Patients with poorly controlled asthma defined as requiring a course of oral or parenteral corticosteroids, admission to hospital for asthma (including treatment in an emergency room), or exacerbation of asthma in the four weeks prior to visit 1 Patients who suffer from seasonal asthma alone or patients who are likely to have a major exacerbation of their asthma due to seasonal effects during the study run-in or treatment period A history of lower airway infection in the four weeks prior to visit 1 A diagnosis of chronic obstructive pulmonary disease (COPD) and/or other relevant lung disease (e.g. cystic fibrosis, bronchiectasis) Heavy smoker currently smoking >20 cigarettes per day and/or >10 pack years or the patient is an ex-smoker who has smoked >10 pack years Patients using >8 puffs/day relief medication regularly prior to visit 1 Clinically relevant abnormal laboratory values suggesting an unknown disease and requiring further clinical evaluation A diagnosis, treatment or remission of any cancer (other than basal cell carcinoma) within two years prior to visit 1 Patients with chronic heart failure class III or IV (New York Heart Association) Suspected hypersensitivity and/or contraindication to any ingredients of the study medication (roflumilast, BDP, or salbutamol) A history of alcoholism or substance abuse within the 12 months prior to visit 1 Pregnancy or women of childbearing potential who are not using a reliable method of contraception
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
AstraZeneca AstraZeneca
Organizational Affiliation
AstraZeneca
Official's Role
Study Director
Facility Information:
Facility Name
ALTANA Pharma
City
Cities in Georgia
State/Province
Georgia
Country
United States
Facility Name
ALTANA Pharma
City
Cities in Austria
Country
Austria
Facility Name
ALTANA Pharma
City
Cities in Croatia
Country
Croatia
Facility Name
ALTANA Pharma
City
Cities in the Czech Repulik
Country
Czech Republic
Facility Name
ALTANA Pharma
City
Cities in Finland
Country
Finland
Facility Name
ALTANA Pharma
City
Cities in France
Country
France
Facility Name
ALTANA Pharma
City
Cities in Greece
Country
Greece
Facility Name
ALTANA Pharma
City
Cities in Hungary
Country
Hungary
Facility Name
ALTANA Pharma
City
Cities in India
Country
India
Facility Name
ALTANA Pharma
City
Cities in Ireland
Country
Ireland
Facility Name
ALTANA Pharma
City
Cities in Italy
Country
Italy
Facility Name
ALTANA Pharma
City
Cities in New Zealand
Country
New Zealand
Facility Name
ALTANA Pharma
City
Cities in Norway
Country
Norway
Facility Name
ALTANA Pharma
City
Cities in Pakistan
Country
Pakistan
Facility Name
ALTANA Pharma
City
Cities in the Philippines
Country
Philippines
Facility Name
ALTANA Pharma
City
Cities in Poland
Country
Poland
Facility Name
ALTANA Pharma
City
Cities in Portugal
Country
Portugal
Facility Name
ALTANA Pharma
City
Cities in the Russian Federation
Country
Russian Federation
Facility Name
ALTANA Pharma
City
Sites in Singapore
Country
Singapore
Facility Name
ALTANA Pharma
City
Cities in South Africa
Country
South Africa
Facility Name
ALTANA Pharma
City
Cities in Spain
Country
Spain
Facility Name
ALTANA Pharma
City
Cities in Taiwan
Country
Taiwan
Facility Name
ALTANA Pharma
City
Cities in Thailand
Country
Thailand
Facility Name
ALTANA Pharma
City
Cities in the United Kindom
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
26612545
Citation
Chervinsky P, Meltzer EO, Busse W, Ohta K, Bardin P, Bredenbroker D, Bateman ED. Roflumilast for asthma: Safety findings from a pooled analysis of ten clinical studies. Pulm Pharmacol Ther. 2015 Dec;35 Suppl:S28-34. doi: 10.1016/j.pupt.2015.11.003. Epub 2015 Nov 22.
Results Reference
derived
PubMed Identifier
26498386
Citation
Meltzer EO, Chervinsky P, Busse W, Ohta K, Bardin P, Bredenbroker D, Bateman ED. Roflumilast for asthma: Efficacy findings in placebo-controlled studies. Pulm Pharmacol Ther. 2015 Dec;35 Suppl:S20-7. doi: 10.1016/j.pupt.2015.10.006. Epub 2015 Oct 21.
Results Reference
derived
Links:
URL
http://filehosting.pharmacm.com/DownloadService.ashx?client=CTR_MED_7111&studyid=4472&filename=BY217-M2-013-RDS-2008-01-21.pdf
Description
BY217-M2-013-RDS-2008-01-21.pdf

Learn more about this trial

Efficacy and Safety of Oral Roflumilast Taken With Low Dose Inhaled Corticosteroids in Patients With Asthma (12 to 70 y) (BY217/M2-013)

We'll reach out to this number within 24 hrs