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Clinical Trials/NCT02161757
NCT02161757
Completed
Phase 3

A Phase 3 Study to Evaluate the Efficacy and Safety of Tralokinumab in Adults and Adolescents With Asthma Inadequately Controlled on Inhaled Corticosteroid Plus Long-Acting β2-Agonist.

AstraZeneca1 site in 1 country1,207 target enrollmentJune 13, 2014

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Uncontrolled Asthma
Sponsor
AstraZeneca
Enrollment
1207
Locations
1
Primary Endpoint
Annualised Asthma Exacerbation Rate (AAER) up to Week 52
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

A 52-Week, Multicentre, Randomized, Double-Blind, Parallel Group, Placebo Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Tralokinumab in Adults and Adolescents with Asthma Inadequately Controlled on Inhaled Corticosteroid Plus Long-Acting β2-Agonist

Detailed Description

This is a randomized, double-blind, parallel group, placebo-controlled study designed to evaluate efficacy and safety of tralokinumab administered subcutaneously in subjects with uncontrolled asthma on inhaled corticosteroid plus long-acting β2-agonist and having a history of asthma exacerbations. Approximately 1140 subjects will be randomized globally. Subjects will receive tralokinumab, or placebo, administered via subcutaneous injection at the study site, over a 52-week treatment period.

Registry
clinicaltrials.gov
Start Date
June 13, 2014
End Date
July 18, 2017
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Documented physician-diagnosed asthma.
  • Documented treatment with ICS at a total daily dose corresponding to ≥500μg fluticasone propionate dry powder formulation equivalents) and a LABA
  • Morning pre-BD FEV1 value of ≥40 and \<80% value (\<90% for patients 12 to 17 years of age) of their PNV.
  • Post-BD reversibility of ≥12% and ≥200 mL in FEV1
  • ACQ-6 score ≥1.5

Exclusion Criteria

  • Pulmonary disease other than asthma
  • History of anaphylaxis following any biologic therapy
  • Hepatitis B, C or HIV
  • Pregnant or breastfeeding
  • History of cancer
  • Current tobacco smoking or a history of tobacco smoking for ≥ 10 pack-years
  • Previous receipt of tralokinumab

Outcomes

Primary Outcomes

Annualised Asthma Exacerbation Rate (AAER) up to Week 52

Time Frame: Baseline (Week 0) up to Week 52

Asthma exacerbation was defined as a worsening of asthma that led to any of the following: * Use of systemic corticosteroids for at least 3 days; a single depo-injectable dose of corticosteroids was considered equivalent to a 3-day course of systemic corticosteroids. * An emergency room (ER) or urgent care (UC) visit (defined as evaluation and treatment for \<24 hours in an ER or UC centre) due to asthma that required systemic corticosteroids (see above). * An inpatient hospitalisation (defined as admission to an inpatient facility and/or evaluation and treatment in a healthcare facility for ≥24 hours) due to asthma. AAER = number of exacerbations\*365.25 / (follow-up date - date of randomisation + 1) (where maximum follow-up time for a patient was approximately 52 weeks). AAER in the tralokinumab group was compared to that seen in the placebo group up to Week 52 using a negative binomial model; rate ratios and rate reductions are both presented for comparative statistical analyses.

Secondary Outcomes

  • Percent Change From Baseline to Week 52 in Pre-dose/Pre-bronchodilator (BD) Forced Expiratory Volume in 1 Second (FEV1)(Baseline (Week 0) and Week 52)
  • Change From Baseline to Week 52 in Asthma Control Questionnaire-6 (ACQ-6) Score(Baseline (Week 0) and Week 52)
  • AAER Associated With an ER/UC Visit, or a Hospitalisation up to Week 52(Baseline (Week 0) up to Week 52)
  • Change From Baseline to Week 52 in Total Asthma Symptom Score (Bi-weekly Means)(Baseline (Week 0) and Week 52)
  • Change From Baseline to Week 52 in Asthma Quality of Life Questionnaire for 12 Years and Older (AQLQ(S)+12) Total Score(Baseline (Week 0) and Week 52)
  • Change From Baseline in European Quality of Life - 5 Dimension 5 Levels (EQ-5D-5L) Visual Analogue Scale (VAS) Scores at Week 52(Baseline (Week 0) and Week 52)
  • Change From Baseline in Total Asthma Rescue Medication Use at Week 52 (Bi-weekly Means)(Baseline (Week 0) and Week 52)
  • Change From Baseline in Home Peak Expiratory Flow (PEF) (Morning and Evening) at Week 52(Baseline (Week 0) and Week 52)
  • Work Productivity and Activity Impairment Questionnaire and Classroom Impairment Questions (WPAI+CIQ): Productivity Loss at Week 52(At Week 52)
  • Change From Baseline in Night-time Awakenings Due to Asthma Requiring Rescue Medication Use at Week 52 (Bi-weekly Means [Percentage])(Baseline (Week 0) and Week 52)
  • Number of Patients With ≥1 Asthma Exacerbation up to Week 52(Baseline (Week 0) up to Week 52)
  • WPAI+CIQ: Activity Impairment at Week 52(At Week 52)
  • Asthma-related Healthcare Encounters by Type up to Week 52(Baseline (Week 0) up to Week 52)
  • Number of Patients Positive for Anti-drug Antibodies (ADAs)(Baseline (Week 0), Week 26, Week 56 (follow-up) and Week 72 (follow-up))
  • Asthma-related Healthcare Encounters by Type up to Week 52: Hospitalisations(Baseline (Week 0) up to Week 52)
  • Asthma-related Healthcare Encounters by Type up to Week 52: Spirometry(Baseline (Week 0) up to Week 52)
  • Serum Trough Concentration (Ctrough) of Tralokinumab During the Study Period up to Week 72(Blood samples were collected pre-dose at Baseline (Week 0), and at Week 4, Week 8, Week 26, Week 52 and Week 72 (follow-up))

Study Sites (1)

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