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Graft-Versus-Host Disease - Opportunity Analysis and Forecasts to 2018
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Transcript of Graft-Versus-Host Disease - Opportunity Analysis and Forecasts to 2018
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OpportunityAnalyzer: Graft-Versus-Host
Disease - Opportunity Analysis and
Forecasts to 2018
Category : Pharma & Healthcare
All logos and Images mentioned on this slide belong to their respective owners.
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Introduction to Report
Launch Date: August 20, 2014
Number of Pages: 252
Geography Coverage: Global
Available Format: PDF
Price For Single User License: USD 5,995
Price For Site User License: USD 11,990
Price For Global User License: USD 17,985
Delivery Time: Within 24 Hours (During Working Days)
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About the Report
The main drivers of growth in graft versus host disease over the 2013-2018 forecast period include the increasing numbers of allogeneic hematopoietic stem cell transplants and the increasing use of biologic off-label and marketed therapies in the 6MM.
Sanofi is a key player in the GVHD market with Thymoglobuline and Lemtrada by infiltrating prophylaxis, aGVHD and cGVHD. Gaining more and more ground in the treatment management of cGVHD is Roche’s Rituxan that Publisher estimates will be one of the bestselling biologics in GVHD in the US by 2018.
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Research Finding
The graft-versus-host disease (GVHD) treatment market value will increase from $297 million in 2013 to $407 million by 2018, at a Compound Annual Growth Rate (CAGR) of 6.59%, according to research.
"OpportunityAnalyzer: Graft-Versus-Host Disease - Opportunity Analysis and Forecasts to 2018" report states that this growth, which will occur over six major markets (6MM: the US, France, Germany, Italy, Spain and the UK), will be strongest in the five European countries (5EU), where multiple product launches will accelerate the market value at a CAGR of 9.26% during the forecast period.
Several products are due to enter the GVHD market by 2018, with Osiris Therapeutics and Mesoblast’s first-to-market Prochymal expected to generate sales of $12.2 million in 2018.
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Key Findings
High uptake of off-label biologics (Rituxan, Lemtrada, Remicade and Thymoglobuline)
No national guidelines are in place
GVHD remains a field of highly unattained unmet need
No consensus over clinical trial endpoints
Regulatory T cells (Tregs) are the focus of the early stage pipeline
Huge opportunity exists in the chronic patient segment of GVHD
Institutionally funded studies are the core of GVHD treatment management
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Report Coverage
1. Introduction
2. Disease Overview
3. Epidemiology
4. Current Treatment Options
5. Unmet Need and Opportunity
6. Research and Development Strategies
7. Pipeline Assessment
8. Pipeline and Off-Label Valuation Analysis
9. Appendix
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