Safety and Efficacy Study of Budesonide (Pulmicort®) Turbuhaler® in Japanese Children With Bronchial Asthma

Asthma Clinical Trial

Official title:

An Open-label, Multi-center, Long Term Study to Investigate the Safety and Efficacy of Budesonide Turbuhaler® Treatment for 48 Weeks (Following 6 Weeks Phase III Study) in Japanese Children With Bronchial Asthma Aged 5 Years to 15 Years Old

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00509028
• Other study ID #: D5254C00006
• Status: Completed
• Phase: Phase 3
• First received: July 17, 2007
• Last updated: July 24, 2012
• Start date: December 2006
• Est. completion date: October 2008

Study information

• Verified date: July 2012
• Source: AstraZeneca
• Contact: n/a
• Is FDA regulated: No
• Health authority: Japan: Ministry of Health, Labor and Welfare
• Study type: Interventional

Clinical Trial Summary

This study will include the patients who are Japanese children with bronchial asthma aged 5 years to 15 years old and have completed the Phase III study (Study code: D5254C00769) at about 29 centres. To investigate the safety of budesonide Turbuhaler® with a daily dose of 100 µg to 800 µg for 54 weeks treatment including the prior 6 weeks Phase III study (Study D5254C00769, NCT00504062) as compared with conventional therapy in Japanese children with bronchial asthma in need of inhaled glucocorticosteroid treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 241
• Est. completion date: October 2008
• Est. primary completion date: October 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 5 Years to 15 Years

Eligibility

Inclusion Criteria:

• Patient who complete preceding the Phase III study and provide a signed written informed consent by patient's legal representative at Visit 1 or 4 weeks prior to Visit 1 of the study. A signed written informed assent should also be obtained from the patients themselves as much as possible

• When the investigator will obtain the signed written informed consent of Phase III study (D5254C00769) from patient's legal representative, the investigator will also provide the information of this study

Exclusion Criteria:

• Respiratory infections that, in the opinion of the investigator(s), may affect the efficacy evaluation e.g., lower airways infection such as pneumonia, infection with no available effective antimicrobial drugs or with deep seated mycosis

• Concurrent serious diseases of liver, kidney, heart or other complications which, in the opinion of the investigator, may either put the patient at risk because of participation in the study, or may influence the results of the study, or the patient's ability to participate in the study. Any clinically relevant abnormal findings in vital sign or physical examination at Visit 1 in this study, which in the opinion of the investigator may put the patient at risk because of his/her participation in the study.

• Pregnant or possible pregnancy or planning to become pregnant during the study period

• Other subjects who are considered inappropriate to participate in this study judged by the investigator

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Asthma

Intervention

Drug:
• Budesonide
Budesonide Turbuhaler 100 mcg (Pulmicort® Turbuhaler®), 100 - 400 mcg daily
• Conventional Asthma Therapy
According to the Japanese Paediatric Guideline for the Treatment and Management of Asthma and at daily dose as judged by the investigator.

Locations

Country	Name	City	State
Japan	Research Site	Takizawa	Iwate

Sponsors (1)

Lead Sponsor	Collaborator
AstraZeneca

Country where clinical trial is conducted

Japan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Patients With Adverse Events (AEs).	AEs were defined as undesirable medical conditions or deteriorations of a pre-existing medical condition following/during exposure. All Serious AEs, AEs leading to withdrawal, Other relevant AE were recorded.	54 weeks	No
Secondary	Number of Patients With Abnormal Clinical Laboratory Test Values.	Analysis of haematological, clinical chemistry and urynalysis variables were performed.; Haematology variables: erythrocytes, haemoglobin, haematocrit, leucocyte count, leucocyte different count (neutrophils, eosinophils, basophils, lymphocytes, monocytes), platelet count.; Clinical chemistry measurements: aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), total bilirubin, albumin, creatinine,sodium, potassium, total protein, blood urea nitrogen.; Urinalysis variables: protein, glucose, urobilinogen, occult.	54 weeks	No
Secondary	Number of Patients With Abnormal Vital Sign Values for the Following Variables: Blood Pressure (Sitting) and Pulse Rate (Sitting), as Judged by the Investigator		54 weeks	No
Secondary	Number of Patients With Abnormal Plasma Cortisol Values.	Cut-off value of cortisol is defined as 4 mcg/dL.	54 weeks	No
Secondary	Height	Height, change from baseline calculated as (height at last visit - height at randomization)	Baseline and 54 weeks	No
Secondary	Weight	Weight, change from baseline calculated as (weight at last visit - weight at randomization)	Baseline and 54 weeks	No
Secondary	Morning Peak Expiratory Flow (PEF) Percentage of Predicted Normal	Change in PEF percent of predicted normal calculated as (PEF percent predicted normal at last visit - PEF percent predicted normal at randomization).	54 weeks	No
Secondary	Change From Baseline of Respiratory Condition at Asthma Attacks (Daytime)	Change in respiratory condition at asthma attacks (daytime) from baseline to last visit. Scale: 0 - 4.; 0 = None. 1 = Mild. 2 = Moderate. 3= Severe. 4 = Respiratory insufficiency	Baseline and 54 weeks	No
Secondary	Change From Baseline of Respiratory Condition at Asthma Attacks (Nighttime)	Change in respiratory condition at asthma attacks (nighttime) from baseline calculated as (respiratory condition at asthma attacks (nighttime) at last visit - respiratory condition at asthma attacks (night-time) at randomization).; Scale: 0 - 4. 0 = None. 1 = Mild. 2 = Moderate. 3= Severe. 4 = Respiratory insufficiency.	Baseline and 54 weeks	No
Secondary	Change From Baseline of Use of Inhaled Short-acting B-2 Agonist (Daytime)	Change in use of inhaled short-acting B-2 agonist (daytime) from baseline calculated as (use of inhaled short-acting B-2 agonist (daytime) at last visit - use of inhaled short-acting B-2 agonist (daytime) at randomization)	Baseline and 54 weeks	No
Secondary	Change From Baseline of Use of Inhaled Short-acting B-2 Agonist (Night-time)	Change in use of inhaled short-acting B-2 agonist (night-time) from baseline calculated as (use of inhaled short-acting B-2 agonist (night-time) at last visit - use of inhaled short-acting B-2 agonist (night-time) at randomization)	Baseline and 54 weeks	No
Secondary	Change From Baseline in Disturbance of Daily Activities	Change in disturbance of daily activities from baseline calculated as (disturbance of daily activities at last visit - disturbance of daily activities at randomization).; Frequency of disturbance of daily activity was assessed using 3- grade scale (normal, almost able, unable).	Baseline and 54 weeks	No
Secondary	Change From Baseline in Disturbance of Night-time Sleep	Change in disturbance of night-time sleep from baseline calculated as (disturbances of night-time sleep at last visit - disturbances of night-time sleep at randomization).; Frequency of disturbance of night- time sleep was assessed using 3- grade scale (normal, almost able, unable).	Baseline and 54 weeks	No
Secondary	Forced Expiratory Volume in One Second (FEV1) Percentage of Predicted Normal Change From Baseline	Forced Expiratory Volume in one second (FEV1) percentage of predicted normal change from baseline calculated as: 100 * (FEV1 at last visit - FEV1 at randomization)/predicted normal FEV1).	54 weeks	No