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Utibron Neohaler

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    Report

  • 22 Pages
  • July 2018
  • Region: Global
  • Citeline
  • ID: 4775389
Drug Overview
Novartis, under license from Vectura and Sosei, developed Utibron, a once-daily long-acting beta 2 agonist/long-acting muscarinic antagonist (LABA/LAMA) combination product containing indacaterol and glycopyrrolate. The company has developed the components as monotherapies, and Arcapta (indacaterol) was the first product of the franchise to gain approval. Utibron received EU and Japanese approvals for use in COPD in September 2013, and launched in Germany and Japan in November 2013, ahead of GlaxoSmithKline’s Anoro ([umeclidinium + vilanterol]). The LABA/LAMA combination received US approval in October 2015.

Table of Contents

OVERVIEW
Drug Overview
Product Profiles
Utibron Neohaler: Chronic obstructive pulmonary disease (COPD)
LIST OF FIGURES
Figure 1: Utibron for COPD – SWOT analysis
Figure 2: The authors drug assessment summary of Ultibro/Utibron for COPD
Figure 3: The authors drug assessment summary of Ultibro/Utibron for COPD
Figure 4: Utibron sales for COPD across the US, Japan, and five major EU markets, by country, 2017–26
LIST OF TABLES
Table 1: Utibron drug profile
Table 2: Utibron Phase III EXPEDITION trial data in COPD
Table 3: Utibron other Phase III data in COPD
Table 4: Utibron sales for COPD across the US, Japan, and five major EU markets, by country ($m), 2017–26