Rare Disease Treatment Market Estimated to exhibit a CAGR of 8.6% during 2017 – 2025
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The report covers important geographies of North America, Latin America, Europe, Asia Pacific and Middle East and Africa. Of these major landscapes, North America lays a significant growth track to show a value of US$ 78,434 Mn by the end of 2025 according to forecast insights in the research study. Following North America, Europe and Asia Pacific, especially Japan, are in line showing potential for the treatment of rare diseases over the period of eight years. The Middle East and Africa region (MEA) will depict sluggish growth owing to low awareness of rare diseases and hence their treatments.
Several opportunities lurk around the market, creating a positive impact on global market growth rate
Acquisitions across the global scenario can be used to expand the business portfolio and operations of key players, who will do well to leverage this strategy to establish a global footprint. Forward integration can be achieved by expanding the value chain. The operating efficiency should be increased to achieve high return on investment. This can be achieved by shifting the manufacturing of important medicines to orphan drugs. The manufacturers of orphan drugs are enjoying the advantages of tax benefits, fast approvals and other research grants, thereby making room for more innovations. Product innovation can lead to advanced therapeutics and innovations in medicine or drugs, which can be used to tap new markets. Moreover, the increasing incidence of rare diseases gives a plus to the market. The public is aware of these rare diseases and this awareness is rising owing to government effort and other social groups. Adding to this scenario, the reimbursement schemes in developed economies are pushing the growth in demand for rare disease treatments and thereby fueling the rare disease treatment market growth in developed countries.
Global Rare Disease Treatment Market: Segmental Forecast
The global rare disease treatment market report involves a five level segmentation comprising – by therapeutic area, by drug type, by drug class, by mode of administration and by distribution channel.
The genetic diseases segment by therapeutic area, which was dominating the global market in the past will show similar traction in the next eight years. This segment is anticipated to be valued at US$ 56,241 Mn by the end of 2025. The metabolic diseases segment by therapeutic type shows higher growth rate as compared to the genetic disease segment and is poised to reach a value of US$ 23,938 Mn by 2025 end
By drug type, originator drugs is the largest segment in the global rare disease treatment market, estimated to hold about 75% market share by 2025 end
Of the various drug class segments, organic compounds is the dominant and most attractive segment, with attractiveness index of 0.6 during the forecast period
The oral segment by mode of administration dominates the global market for rare disease treatment from a revenue standpoint and is forecasted to continue this trait throughout the period of forecast. It has the highest market attractiveness index of 2.2. The injectable segment is poised to account for a value share of 39.5% by 2025 end and reflects a market attractiveness index of 0.8
By distribution channel, specialty pharmacies segment dominated the global rare disease treatment market in revenue terms in 2016 and is projected to continue to do so throughout the forecast period. Specialty pharmacies is the most attractive segment, with attractiveness index of 1.6 during the forecast period
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Competitive Intelligence – Key Player Analysis
The research report on the global rare disease treatment market profiles key players in the market and their complete intelligence including facts such as product portfolio, strategies, geographical spread, etc. Some of the key players involved are Novartis AG, Pfizer, F. Hoffmann-La Roche Ltd., Celgene Corporation, AbbVie Inc., Johnson & Johnson Services, Inc., Shire, Alexion, Novo Nordisk A/S, Sanofi, Bayer AG, Amgen, Inc., Allergan plc., Eisai Co. Ltd., Bristol-Myers Squibb Company, Merck & Co., Inc., Vertex Pharmaceuticals, Baxter, BioMarin and Teva Pharmaceutical Industries Ltd.
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