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Synagis (Pediatric RSV) - Comparative Analysis, Shares and Latest Updates Report to 2022

(Medical-NewsWire.com, February 24, 2016 ) Synagis (Pediatric RSV) - Forecast and Market Analysis to 2022 Size and Share Published in 2013-04-30 Available for US$ 3495 at Researchmoz.us

Description

To Browse a Full Report at: http://www.researchmoz.us/synagis-pediatric-rsv-forecast-and-market-analysis-to-2022-report.html


GlobalData has released its new PharmaPoint Drug Evaluation report, Synagis (Pediatric RSV) Forecast and Market Analysis to 2022. Respiratory syncytial virus (RSV) is a common cause of pediatric respiratory infections and virtually all children will have been infected by the virus by the age of two. RSV transmission typically occurs during the winter and early spring months. The virus is spread through the air by an infected persons sneeze or cough, or through direct and indirect contact with nasal secretions of an infected person. The majority of RSV infections present as mild upper respiratory illnesses that often self-resolve within two weeks, but about 1% of the cases develop serious lower respiratory complications requiring hospitalization. Children under the age of two with certain health conditions are most at risk for severe RSV infections and are therefore recommended to receive RSV prophylaxis treatments. The only FDA-approved prophylactic intervention in the US is AstraZenecas Synagis (palivizumab), a humanized monoclonal antibody against the fusion protein of the virus.

AstraZenecas Synagis (palivizumab) is a humanized mouse mAb used for the prevention of serious lower respiratory tract disease as a result of RSV infection in high-risk pediatric patients under the age of two. Synagis mechanism of action involves the binding of the antibody to the viral F protein. Synagis received FDA approval in 1998, and by 2002 was approved in all the seven major markets (7MM) (US, France, Italy, Germany, Spain, UK, and Japan) for the prophylaxis of infants at high risk of severe RSV infection. Today, Synagis is approved in 83 countries worldwide (AstraZeneca, 2012). Synagis is the only immunoprophylaxis approved for pediatric patients.

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Scope

Overview of RSV, including epidemiology, etiology, symptoms, diagnosis, pathology and treatment guidelines as well as an overview on the competitive landscape.

Detailed information on Synagis including product description, safety and efficacy profiles as well as a SWOT analysis.

Sales forecast for Synagis for the US from 2012 to 2022.

Sales information covered for the US

Reasons to buy

Understand and capitalize by identifying products that are most likely to ensure a robust return

Stay ahead of the competition by understanding the changing competitive landscape for RSV

Effectively plan your M&A and partnership strategies by identifying drugs with the most promising sales potential

Make more informed business decisions from insightful and in-depth analysis of Synagis performance

Obtain sales forecast for Synagis from 2012-2022 the US

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Table of Content

1 Table of Contents

1 Table of Contents 7

1.1 List of Tables 9

1.2 List of Figures 9


2 Introduction 10

2.1 Catalyst 10

2.2 Related Reports 10

3 Disease Overview 11

3.1 Etiology and Pathophysiology 11

3.1.1 Pathophysiology 15

3.1.2 Prognosis 16

3.1.3 Quality of Life 16

3.2 Symptoms 17

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