跳至主要内容
临床试验/NCT02258542
NCT02258542已完成3 期

A Multicentre, Double-blind, Randomized, Parallel Group, Phase 3 Safety Extension Study to Evaluate the Safety and Tolerability of Benralizumab (MEDI-563) in Asthmatic Adults and Adolescents on Inhaled Corticosteroid Plus Long-acting β2 Agonist (BORA)

AstraZeneca432 个研究点 分布在 2 个国家目标入组 2,133 人开始时间: 2014年11月19日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
AstraZeneca
入组人数
2,133
试验地点
432
主要终点
Change From Baseline in Basophils, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

研究概览

简要总结

The purpose of this study is to characterize the safety profile of benralizumab administration in asthma patients who have completed one of the three predecessor studies: D3250C00017, D3250C00018 or D3250C00020.

详细描述

After a minimum of 1200 patients have been enrolled in this study, subsequent patients (up to a maximum of 2200 total for the study), who complete a minimum of 16 weeks, and no more than 40 weeks, in this study, will be given the option to transition to an open-label safety extension study, Study D3250C00037 (MELTEMI).

Adolescent patients, patients from Japan and South Korea, and any patient who chooses not to enter Study D3250C00037 will remain in this study through IPD or EOT and FU.

At the time of the first interim analysis in Japanese patients, the study regimen for all patients will become unblinded to AstraZeneca for data analysis purposes. Study conduct and blinding at the site and patient level will remain unchanged.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Investigator)

入排标准

年龄范围
12 Years 至 75 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Benralizumab Arm B

Experimental

Benralizumab administered subcutaneously

干预措施: Benralizumab (Biological)

Benralizumab Arm A

Experimental

Benralizumab administered subcutaneously

干预措施: Benralizumab (Biological)

结局指标

主要结局

Change From Baseline in Basophils, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of Basophils.

Change From Baseline in Lymphocytes, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of Lymphocytes.

Change From Baseline in Basophils, Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in hematologic lab parameter of Basophils.

Change From Baseline in Leukocytes, Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in hematologic lab parameter of Leukocytes.

Change From Baseline in Leukocytes, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of Leukocytes.

Change From Baseline in Lymphocytes, Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in hematologic lab parameter of Lymphocytes.

Change From Baseline in Neutrophils, Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in hematologic lab parameter of Neutrophils.

Change From Baseline in Neutrophils, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of Neutrophils.

Change From Baseline in Eosinophils, Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in hematologic lab parameter of Eosinophils.

Change From Baseline in Eosinophils, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of Eosinophils.

Change From Baseline in Alanine Aminotransferase (ALT), Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in chemistry tests ALT.

Change From Baseline in ALT, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of ALT.

Change From Baseline in Aspartate Aminotransferase (AST), Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in chemistry tests AST.

Change From Baseline in AST, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of AST.

Change From Baseline in Bilirubin, Full Analysis Set, Excluding MELTEMI Patients

时间窗: Week 56

Change from baseline in chemistry test Bilirubin.

Change From Baseline in Bilirubin, Full Analysis Set, Adolescents Only (SIROCCO/CALIMA)

时间窗: Week 108

Change from baseline in hematologic lab parameter of Bilirubin.

次要结局

  • Number of Overall Patients With Asthma Exacerbations During Study Period(From week 0 to week 56 in study treatment period and through the follow up period (16 weeks from day of last dose))
  • Number of Overall Patients With Asthma Exacerbations During Study Period, Adolescents Only (SIROCCO/CALIMA)(From week 0 to week 108 in study treatment period and through the follow up period (16 weeks from day of last dose))
  • Change From Baseline in Pre-bronchodilator FEV1 (L)(Week 56)
  • Change From Baseline in Pre-bronchodilator FEV1 (L), Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Classroom Productivity Loss Using Classroom Impairment Questionnaire (CIQ)(Week 56)
  • Change From Baseline in Post-bronchodilator FEV1 (L)(Week 56)
  • Change From Baseline in Asthma Control Questionnaire (ACQ) as a Measure of Asthma Control in Overall Patients(Week 56)
  • Change From Baseline in Asthma Control Questionnaire (ACQ) as a Measure of Asthma Control in Overall Patients, Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Change From Baseline in Total Score of Asthma Related and General Health-related Quality of Life Questionnaire (AQLQ(S)+12)(Week 56)
  • Change From Baseline in Total Score of Asthma Related and General Health-related Quality of Life Questionnaire (AQLQ(S)+12), Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Change From Baseline in EQ-5D-5L Visual Analog Scale, Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Work Productivity Loss in Adults, Using Work Productivity and Activity Impairment Questionnaire (WPAI), Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Classroom Productivity Loss Using Classroom Impairment Questionnaire (CIQ), Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Number of Patients Who Had Health Care Encounter (ie, Hospitalization, Emergency Department Visits, Urgent Care Visits, and All Other Outpatient Visits Due to Asthma) During Study Period(From week 0 to week 68 in study treatment period and through the follow up period (16 weeks from day of last dose))
  • Pre-dose Benralizumab Concentration in Serum During the Treatment Phase of the Safety Study(Week 0 and Week 56)
  • Number of Patients With Anti-drug Antibodies (ADA) Responses During the Study, Adolescents Only (SIROCCO/CALIMA)(From week 0 to week 108 study treatment period (adults) and plus 16 weeks the follow up period; From week 0 to week 108-week in study treatment period (adolescents) and plus 16 weeks the follow up period)
  • Change From Baseline in Post-bronchodilator FEV1 (L), Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Change of Blood Eosinophil Levels' Measurement in Overall Patients(Week 56)
  • Change of Blood Eosinophil Levels' Measurement in Adolescents Patients (SIROCCO/CALIMA).(Week 108)
  • Change From Baseline in EQ-5D-5L Visual Analog Scale(Week 56)
  • Work Productivity Loss in Adults, Using Work Productivity and Activity Impairment Questionnaire (WPAI)(Week 68)
  • Activity Impairment (%), Using Work Productivity and Activity Impairment Questionnaire (WPAI)(Week 68)
  • Number of Patients With Anti-drug Antibodies (ADA) Responses During the Study(From week 0 to week 56 in study treatment period (adults) and plus 16 weeks the follow up period; From week 0 to week 108-week in study treatment period (adolescents) and plus 16 weeks the follow up period)
  • Activity Impairment (%), Using Work Productivity and Activity Impairment Questionnaire (WPAI), Adolescents Only (SIROCCO/CALIMA)(Week 108)
  • Number of Patients Who Had Health Care Encounter (ie, Hospitalization, Emergency Department Visits, Urgent Care Visits, and All Other Outpatient Visits Due to Asthma) During Study Period, Adolescents Only (SIROCCO/CALIMA)(Baseline and Week 108)
  • Pre-dose Benralizumab Concentration in Serum During the Treatment Phase of the Safety Study, Adolescents Only (SIROCCO/CALIMA)(Baseline and Week 108)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (432)

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