Sponsor Novartis Pharmaceuticals



Similar documents
This clinical study synopsis is provided in line with Boehringer Ingelheim s Policy on Transparency and Publication of Clinical Study Data.

This clinical study synopsis is provided in line with Boehringer Ingelheim s Policy on Transparency and Publication of Clinical Study Data.

Sponsor. Novartis Generic Drug Name. Vildagliptin. Therapeutic Area of Trial. Type 2 diabetes. Approved Indication. Investigational.

Sponsor Novartis. Generic Drug Name Secukinumab. Therapeutic Area of Trial Psoriasis. Approved Indication investigational

Longitudinal Modeling of Lung Function in Respiratory Drug Development

Bronchodilators in COPD

FREEDOM C: A 16-Week, International, Multicenter, Double-Blind, Randomized, Placebo-Controlled Comparison of the Efficacy and Safety of Oral UT-15C

Before prescribing for COPD management, the patient should have had appropriate assessment, including spirometry, as per NICE guidelines.

Medical Policy An independent licensee of the Blue Cross Blue Shield Association

Clinical Study Synopsis

Clinical Study Synopsis

1.0 Abstract. Title: Real Life Evaluation of Rheumatoid Arthritis in Canadians taking HUMIRA. Keywords. Rationale and Background:

2.0 Synopsis. Vicodin CR (ABT-712) M Clinical Study Report R&D/07/095. (For National Authority Use Only) to Part of Dossier: Volume:

COPD PROTOCOL CELLO. Leiden

Clinical Study Synopsis for Public Disclosure

SYNOPSIS. 2-Year (0.5 DB OL) Addendum to Clinical Study Report

CLINICAL STUDY REPORT SYNOPSIS

Journal Club: Niacin in Patients with Low HDL Cholesterol Levels Receiving Intensive Statin Therapy by the AIM-HIGH Investigators

SYNOPSIS. Risperidone: Clinical Study Report CR003274

Compare the physiologic responses of the respiratory system to emphysema, chronic bronchitis, and asthma

Clinical Study Synopsis

Version History. Previous Versions. Drugs for MS.Drug facts box fingolimod Version 1.0 Author

Riociguat Clinical Trial Program

Prevention of Acute COPD exacerbations

medicineupdate to find out more about this medicine

Exploratory data: COPD and blood eosinophils. David Price: am

Prof. Florian Gantner. Vice President Respiratory Diseases Research Boehringer Ingelheim

COPD and Asthma Differential Diagnosis

Clinical Study Synopsis

Outcome of Drug Counseling of Outpatients in Chronic Obstructive Pulmonary Disease Clinic at Thawangpha Hospital

Pathway for Diagnosing COPD

Presented by: Jean Yoo-Campbell, Matthew Konerman, Monica Konerman, Jean Yoo Campbell, Christian Gocke, Eunpi Cho Donald Lynch

TEMPLATE DATA MANAGEMENT PLAN

Drug therapy SHORT-ACTING BETA AGONISTS SHORT-ACTING ANTICHOLINERGICS LONG-ACTING BETA AGONISTS LONG-ACTING ANTICHOLINERGICS

Interpretation of Pulmonary Function Tests

Humulin (LY041001) Page 1 of 1

Clinical Trial Results Database Page 1

2. Background This drug had not previously been considered by the PBAC.

5. Treatment of Asthma in Children

The submission positioned dimethyl fumarate as a first-line treatment option.

CURRICULUM VITAE KIRK GEORGE VOELKER, M.D.

TUTORIAL on ICH E9 and Other Statistical Regulatory Guidance. Session 1: ICH E9 and E10. PSI Conference, May 2011

Week 12 study results

Pragmatic Seamless Design for Efficacy Trial of Asthma Management with reduced Cost. Mei Lu, PhD Christine Joseph, Ph.D

Comparison/Control Groups. Mary Foulkes, PhD Johns Hopkins University

GEORGIA MEDICAID FEE-FOR-SERVICE ASTHMA and COPD AGENTS PA SUMMARY

Severe asthma Definition, epidemiology and risk factors. Mina Gaga Athens Chest Hospital

Clinical Study Synopsis

PROTOCOL SYNOPSIS Evaluation of long-term opioid efficacy for chronic pain

Management of exacerbations in chronic obstructive pulmonary disease in Primary Care

Version History. Previous Versions. Policy Title. Drugs for MS.Drug facts box Glatiramer Acetate Version 1.0 Author

RES/006/APR16/AR. Speaker : Dr. Pither Sandy Tulak SpP

Standardizing the measurement of drug exposure

COPD RESOURCE PACK SECTION 11. Fife Integrated COPD Care Pathways

Medication Policy Manual. Topic: Aubagio, teriflunomide Date of Origin: November 9, 2012

A Phase 2 Study of Interferon Beta-1a (Avonex ) in Ulcerative Colitis

Idiopathic Pulmonary Fibrosis (IPF) Research

Subject: No. Page PROTOCOL AND CASE REPORT FORM DEVELOPMENT AND REVIEW Standard Operating Procedure

Pharmacology of the Respiratory Tract: COPD and Steroids

Two-Year Phase III Data Presented at AAN 61st Annual Meeting Show Positive Outcome of Cladribine Tablets in Patients with Multiple Sclerosis

CURRICULUM VITAE GREGORY JAMES FERREIRA M.D., FCCP

Acknowledgements. PAH in Children: Natural History. The Sildenafil Saga

PEER REVIEW HISTORY ARTICLE DETAILS

Clinical Guideline. Recommendation 3: For stable COPD patients with respiratory symptoms

Antipsychotic drugs are the cornerstone of treatment

Effect of liraglutide on body weight in overweight or obese subjects with type 2 diabetes: SCALE - Diabetes

Clinical Guideline. Recommendation 3: For stable COPD patients with respiratory symptoms

Best Practices in Managing Patients With Chronic Obstructive Pulmonary Disease (COPD)

Clinical Study Synopsis

Classifying Asthma Severity and Initiating Treatment in Children 0 4 Years of Age

Version History. Previous Versions. for secondary progressive MS (SPMS) Policy Title. Drugs for MS.Drug facts box Interferon beta 1b

ABSTRACT INTRODUCTION PATIENT PROFILES SESUG Paper PH-07

Core therapeutic areas

Achieving Quality and Value in Chronic Care Management

National MS Society Information Sourcebook

COPD Prescribing Guidelines

Pulmonary Rehabilitation in Newark and Sherwood

Irish Association for Emergency Medicine (IAEM) submission to the National COPD Strategy

Statistics and Pharmacokinetics in Clinical Pharmacology Studies

Chronic Obstructive Pulmonary Disease: Developing Drugs for Treatment Guidance for Industry

Guideline on the clinical investigation of medicinal products for the treatment of asthma

Medical management of CHF: A New Class of Medication. Al Timothy, M.D. Cardiovascular Institute of the South

Cost-effectiveness of Pirfenidone (Esbriet ) for the treatment of Idiopathic Pulmonary Fibrosis.

Active centers: 2. Number of patients/subjects: Planned: 20 Randomized: Treated: 20 Evaluated: Efficacy: 13 Safety: 20

Summary of the risk management plan (RMP) for Orkambi (lumacaftor and ivacaftor)

ABOUT XARELTO CLINICAL STUDIES

The Consequences of Missing Data in the ATLAS ACS 2-TIMI 51 Trial

Guidance for Industry FDA Approval of New Cancer Treatment Uses for Marketed Drug and Biological Products

Avastin in Metastatic Breast Cancer

Trial Description. Organizational Data. Secondary IDs

Deaths from Respiratory Diseases: Implications for end of life care in England. June

Investor News. Phase III J-ROCKET AF Study of Bayer s Xarelto (rivaroxaban) Meets Primary Endpoint. Not intended for U.S.

NCT sanofi-aventis HOE901_3507. insulin glargine

STUDY PROGRESS AND SAFETY MONITORING PLAN TEMPLATE

Application Type NDA Submission Number (S-040) and (S-007) Submission Code Supplement

Transcription:

Clinical Trial Results Database Page 1 Sponsor Novartis Pharmaceuticals Generic Drug Name Indacaterol Therapeutic Area of Trial Chronic Obstructive Pulmonary Disease (COPD) Indication studied: COPD Study Number CQAB149B2335S Title A 26-week treatment, multicenter, randomized, double blind, double dummy, placebo-controlled, adaptive, seamless, parallel-group study to assess the efficacy, safety and tolerability of two doses of indacaterol (selected from 75, 150, 300 & 600 μg o.d.) in patients with chronic obstructive pulmonary disease using blinded formoterol (12 μg b.i.d) and open label tiotropium (18 μg o.d.) as active controls Phase of Development Phase II/III Study Start/End Dates 23 Apr 2007 to 23 Aug 2008 Study Design/Methodology This study was a multicenter, double-blind, randomized, placebo and active controlled, adaptive and seamless, parallel-group study design consisting of 2 stages: a dose selection stage from which 2 out of 4 indacaterol doses were selected (150 and 300 µg once daily [o.d.] were selected) following interim analysis to continue into a second stage for comparisons of efficacy, safety and tolerability for up to 26 weeks total treatment. Centres 334 centers in 11 countries: Argentina (6), Canada (24), Germany (35), India (13), Italy (16), Korea (13), Spain (21), Sweden (6), Turkey (8), Taiwan (7), United States (185) Publication Ongoing

Clinical Trial Results Database Page 2 Objectives Primary objective(s) To demonstrate superiority of at least one of the selected doses of indacaterol (150 and 300 μg o.d.) to placebo with respect to 24 h post dose (trough) forced expiratory volume in 1 second (FEV 1 ) after 12 weeks of treatment in patients with COPD. Secondary objective(s) To demonstrate non-inferiority of at least one of the selected doses of indacaterol (150 and 300 μg o.d.) to open label tiotropium (18 μg o.d.) with respect to 24 h post dose (trough) FEV 1 following 12 weeks of treatment. To evaluate the effect of indacaterol (150 or 300 μg o.d.) to placebo on percentage of days of poor control reported over the 26 week randomized treatment period Safety objective(s): Included: To assess the safety and tolerability of indacaterol (150 or 300 μg o.d.) in terms of adverse events Test Product (s), Dose(s), and Mode(s) of Administration Indacaterol 75, 150, 300 and 600 μg o.d., administered once daily by the orally inhaled route via single dose dry powder inhaler (SDDPI) Reference Product(s), Dose(s), and Mode(s) of Administration Formoterol delivered via Aerolizer (Stage 1 only) Tiotropium (18 μg) dry powder capsules delivered via manufacturer s proprietary inhalation device (Handihaler ) Placebo to indacaterol delivered via SDDPI Placebo to formoterol delivered via Aerolizer Criteria for Evaluation Primary variables Trough FEV1 after 12 weeks of treatment Secondary variables Percentage of COPD 'days of poor control' over 26 weeks Safety and tolerability Included monitoring and recording all adverse events (AEs) and serious adverse events (SAEs) Statistical Methods Trough FEV 1 was analyzed using a mixed model containing treatment as a fixed effect with the baseline FEV 1 measurement, FEV 1 prior to inhalation and FEV 1 30 min post inhalation of salbutamol/albuterol (components of SABA reversibility at Day -14), FEV 1 prior to inhalation and

Clinical Trial Results Database Page 3 FEV 1 one hour post inhalation of ipratropium (components of anti-cholinergic reversibility at Day -13) as covariates. To reflect the randomization scheme the model included also the smoking status (current/ex-smoker) and country as fixed effects with center nested within country as a random effect. Estimates of adjusted treatment effects and of treatment contrasts were displayed along with the associated confidence intervals. The percentage of days of poor control was summarized by treatment and analyzed using the same mixed model as specified for the primary analysis, with baseline percentage of days of poor control used instead of baseline FEV 1. Study Population: Inclusion/Exclusion Criteria and Demographics Inclusion criteria: Male and female adults aged 40 years, with a diagnosis of COPD according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) guidelines 2005 and: Smoking history of at least 20 pack-years Post-bronchodilator FEV 1 <80% and 30% of the predicted normal value Post-bronchodilator FEV 1 /FVC (forced vital capacity) <70% (Post refers to within 30 min after inhalation of 400 μg of salbutamol) Key exclusion criteria: Patients who were hospitalized for a COPD exacerbation in the 6 weeks prior to screening Patients who had a respiratory tract infection within 6 weeks prior to screening Patients with concomitant pulmonary disease Patients with a history of asthma Patients with diabetes Type I or uncontrolled diabetes Type II Any patient with lung cancer or a history of lung cancer Patients with a history of certain cardiovascular co-morbid conditions

Clinical Trial Results Database Page 4 Number of Subjects Patient disposition

Clinical Trial Results Database Page 5 Demographic and Background Characteristics (treatments continued into Stage 2)

Clinical Trial Results Database Page 6 Primary Objective Results Trough FEV 1 (L) at Week 12 (imputed with LOCF): treatment comparisons (ITT population)

Clinical Trial Results Database Page 7 Secondary Objective Results Trough FEV 1 (L) at Week 12 (imputed with LOCF): treatment comparisons (ITT population) See the primary objective results table for indacaterol tiotropium comparisons Percentage of COPD days of poor control over 26 weeks: treatment comparisons (ITT population)

Clinical Trial Results Database Page 8 Safety Results Adverse events (including COPD exacerbations) overall and by primary system organ class - n (%) of patients (Safety population, treatments continued into Stage 2)

Clinical Trial Results Database Page 9 Serious Adverse Events and Deaths Deaths, other serious adverse events (including COPD exacerbations) and adverse events leading to permanent discontinuation of study drug n (%) of patients (Safety population, treatments continued into Stage 2) Date of Clinical Trial Report 03 Nov 2008 Date Inclusion on Novartis Clinical Trial Results Database 14 Aug 2009 Date of Latest Update 16 Dec 2009