Press release
Evolving Trend of Orphan Drugs to Drive Rare Neurological Disease Treatment Market Through 2028, Fact.MR Study
The recently published market study by Fact.MR highlights the current trends that are expected to influence the dynamics of the Rare Neurological Disease Treatment Market in the upcoming years.Click here to Get Complete Synopsis of the Report - https://www.factmr.com/report/4594/rare-neurological-disease-treatment-market
The report introspects the supply chain, cost structure, and recent developments pertaining to the Rare Neurological Disease Treatment Market in the report and the impact of the COVID-19 on these facets of the market. Further, the micro and macro-economic factors that are likely to impact the growth of the Rare Neurological Disease Treatment Market are thoroughly studied in the presented market study.
The global rare neurological disease treatment market is anticipated to reach a value pool of ~US$7.5 Bn by 2020 and is projected to grow at Y-o-Y of over 8.5% by 2020 over 2019. The market for rare neurological disorder treatment is expected to follow an upward growth trend over the forecast period on the back of increasing trend of e-prescribed drugs, promotional programmes and regulatory exclusivity.
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The new business model to invest more in orphan drugs developments could offer an integrated healthcare solution that enables pharmaceutical companies to develop newer areas of therapeutics, diagnosis, treatment, monitoring, and patient support. In addition, increasing penetration of online pharmacies is also becoming a wish list of key manufacturers to drive revenue in the rare neurological disease treatment market.
Key Takeaways from the Rare Neurological Disease Treatment Market:
• In terms of revenue, North America accounts for ~40% of the market share in the global rare neurological disease treatment market
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• In East Asia, three countries namely Japan, Taiwan and South Korea have introduced policies that foster orphan drug research and development. Resultantly, the region is expected to witness a strong growth of over 8% during the forecast period (2018-2028).
• Increasing per capita healthcare spending on rare neurological diseases such as Alzheimer’s is supporting the robust growth of the global rare neurological disease treatment market. Healthcare spending on Alzheimer’s disease treatment is poised to create an absolute $ opportunity of more than US$ 5 Bn during the forecast period.
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• The retail pharmacy and drug store segment continues to set a high standard to achieve superior rates of customer satisfaction and is projected to grow at a Y-o-Y of 9% through the forecast period
“Strategic partnerships between pharmaceutical giants and researchers as well as orphan drug legislations are providing financial incentives for companies developing drugs for rare neurological diseases”, Says an Analyst at Fact.MR
Read More Trending and Similar Reports from Fact.MR – http://www.globenewswire.com/en/news-release/2019/04/01/1790807/0/en/Lewy-Body-Dementia-Treatment-Market-Driven-by-Surging-Cholinesterase-Inhibitor-Sales-Fact-MR-Study.html
Market Players Consolidating with Widening Investment Opportunities
The global rare neurological disease treatment market is consolidated across the legacy regions and witnessing several new investments and entry of new manufacturers in key therapeutic areas owing to increasing prevalence of rare diseases. Key Players such as Pfizer, Inc., Johnson & Johnson Services, Inc. and Novartis AG are continuously emphasizing on new investments and R&D activities to reduce their manufacturing costs.
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Over the years, the global market for rare neurological disease treatment has witnessed several collaborations and partnerships between the drug manufacturers to enhance revenue generation and expand geographical drug footprints. This has created several growth opportunities for manufacturers to increase their share in the rare neurological disease treatment market.
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Content Source: https://www.factmr.com/media-release/1367/global-rare-neurological-disease-treatment-market
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