Prominent pharmaceutical companies are emphasizing on major drug development campaigns, conducting extensive clinical trials and laboratory experiments, expected to contribute to future growth
Prominent pharmaceutical companies are emphasizing on major drug development campaigns, conducting extensive clinical trials and laboratory experiments, expected to contribute to future growth
Fact.MR, Rockville MD: The global skeletal dysplasia market is expected to yield substantial gains through 2021, as regulatory authorities around the world fast track approvals of potential drug candidates, according to an ongoing study being conducted by research firm Fact.MR. Long-term projections also appear optimistic, with a robust growth rate likely to prevail through 2031.
Growth is largely expected to be underpinned by extensive research for treating achondroplasia. Being the most frequent type of short-limbed dwarfism, achondroplasia affects at least 1 in 15,000 to 40,000 newborn infants worldwide. However, rates of incidences vary with different geographies. For instance, there is at least 1 case in every 6400 births across Denmark, and 1 in every 10000 births in Latin America.
Key pharmaceutical giants are capitalizing on furthering research on new drug candidates. A case in point is of Astellas Pharma Inc. which, in December 2020, partnered with the Noriyuki Tsumaki Laboratory to develop the ASP5878 candidate. Likewise, in 2019, Ascendis Pharma A/S announced the conferment of orphan drug status for its TransCon C-Type Natriuretic Peptide (CNP) to treat achondroplasia. Such developments are expected to bolster expansion prospects in the long-run.
“As the global pandemic crisis incidence recedes, the global healthcare fraternity is recalibrating its research and development priorities, providing major impetus to studies concerning future skeletal dysplasia drug candidates, opening up possible revenue ecosystems in the long-run,” comments the Fact.MR analyst.
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Key Takeaways from Fact.MR’s Skeletal Dysplasia Market Study
- By disease type, treatment for achondroplasia is likely to emerge as the most promising research area
- Patients to exhibit significant tilt towards growth hormones based skeletal dysplasia treatment
- US to receive credible impetus, driven by ongoing clinical trials for verifying efficacy of drug candidates such as vosoritide
- High incidence of dwarfism to heighten skeletal dysplasia treatment research across the UK
- Germany making significant strides, especially with regard to prenatal sonographic diagnosis for providing timely treatment
- India and China to emerge as attractive growth hotspots, driven by increased healthcare infrastructure development
Skeletal Dysplasia Market- Prominent Drivers
- Heightening government funding for drug development and research is driving skeletal dysplasia treatment growth
- Manufacturers are deploying a combination of hormonal-cum-medicinal treatment, opening up numerous growth opportunities
- Healthcare experts are touting spinal fusion and decompression procedures, promoting heightened research in skeletal dysplasia treatment
Skeletal Dysplasia Market- Key Restraints
- Limited availability of potential drug candidates is hampering skeletal dysplasia market growth
- Prolonged approval schedules from regulatory authorities are delaying new therapeutic approaches availability
Discover more about the skeletal dysplasia market with figures, data tables and the table of contents. You will also find detailed market segmentation on https://www.factmr.com/report/3144/skeletal-dysplasia-market
Competitive Landscape
Key players operating in the skeletal dysplasia market include Dr. Reddy’s Laboratories, Celgene Corporation, Cipla Inc., Novartis AG, Teva Pharmaceutical Industries, Merck Group, F. Hoffmann-La Roche AG, Eli Lilly, Abbott Laboratories, Clementia Pharmaceuticals, Regeneron Pharmaceuticals Inc., and BioMarin Pharmaceuticals Inc. among others.
Manufacturers are concentrating on capacity expansion approaches by relying on strategic moves such as acquisitions, partnerships and collaborations. For instance, in April 2019, Ipsen acquired Clementia Pharmaceuticals, with the objective of expanding its polovarotene drug candidate portfolio, used to treat adult and pediatric rare bone disorders.
Recently, in November 2020, the US Food & Drug Administration accepted the New Drug Application (NDA) for vosoritide, an investigational once daily injection analog of the C-type Natriuretic Peptide (CNP) for children with achondroplasia, the most prominent type of skeletal dysplasia responsible for inducing dwarfism amongst individuals. The approval status is likely to be conferred by August 2021.
More Insights on the Skeletal Dysplasia Market
In its latest report, Fact.MR offers unbiased analysis of the global skeletal dysplasia market. In order to understand the global market potential, its growth, and scope, the market is segmented on the basis of disease type (thanatophoric dysplasia, campomelic dysplasia, achondroplasia, osteogenesis imperfecta, achondrogenesis and others), treatment type (growth hormones, parathyroid hormones, mast cell inhibitors and muscle relaxants) and distribution channel (hospital pharmacies, retail pharmacies, drug stores and online pharmacies) across five regions (North America, Latin America, Europe, Asia-Pacific and Middle East & Africa)
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