Press release
Growth prospects of the Hemophilia Gene Therapy Market Analysis Report
"The Report Hemophilia Gene Therapy - A Pipeline Analysis Report provides information on pricing, market analysis, shares, forecast, and company profiles for key industry participants. - MarketResearchReports.biz"Hemophilia Gene Therapy: An insight
Hemophilia is an inherited bleeding disorder. The gene responsible for hemophilia is present on the X chromosome and is inherited in a recessive manner. Hemophilia A, also called as factor VIII (FVIII) deficiency or classic hemophilia, is caused by missing or defective factor VIII. Most individuals, roughly 85%, have hemophilia A and produce too little or no factor VIII. On the other hand, hemophilia B, which is also called Christmas disease, is caused by a deficiency of factor IX.
Shire became the biggest hemophilia player after it bought Baxalta in June 2016, and the company reported total hemophilia revenue of $870.9 million in the FY 2016.
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Covered in this report
The report covers the present scenario and the growth prospects of the hemophilia gene therapy. The report presents a detailed picture of the market by way of study, synthesis, and summation of data from multiple sources.
Technavio's Hemophilia Gene Therapy - A Pipeline Analysis Report, has been prepared based on an in-depth market analysis with inputs from industry experts. The report covers the market landscape and its growth prospects during the forecast period. The report also includes a discussion of the key companies operating in this market.
Major companies
uniQure
Alnylam Pharmaceuticals
BioMarin Pharmaceutical
Spark Therapeutics
Shire
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Key questions answered in this report
How will the market evolve during the forecast period?
What are the major parameters impacting the market?
What are the key market trends?
What are the challenges to market growth?
Who are the key companies in this market space?
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Table of Contents
PART 01: EXECUTIVE SUMMARY
PART 02: RESEARCH METHODOLOGY
PART 03: HEMOPHILIA GENE THERAPY: AN INSIGHT
Introduction
PART 04: MAJOR REGULATORY AUTHORITIES
US
Europe
Japan
Australia
China
PART 05: PIPELINE LANDSCAPE
PART 06: COMPARATIVE ANALYSIS
Late-stage molecules (Phase III)
Mid-stage molecules (Phase I/II)
Early-stage molecules (Phase I and IND)
Pre-clinical stage molecules
Discontinued molecules
PART 07: INDICATION ANALYSIS
PART 08: THERAPEUTIC ASSESSMENT BY THERAPY
Therapeutic assessment based on therapy
PART 09: THERAPEUTIC ASSESSMENT BY ROA
Therapeutic assessment based on RoA
PART 10: THERAPEUTIC ASSESSMENT BY STAGE AND ROA
Therapeutic assessment based on RoA in various stages of development
PART 11: KEY COMPANIES
Active companies: Category and parameters
PART 12: APPENDIX
List of abbreviations
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