(PharmaNewsWire.Com, September 23, 2021 ) Netherton syndrome is considered to be a hereditary as it is an autosomal recessive trait. It is majorly caused due to mutations associated with SPINK5 gene. In few cases, although there is no family history of the disease, the syndrome is revealed even when two healthy parents that carry the mutated recessive gene have a child, which receives both copies of the recessive gene. The Global Netherton syndrome market is expected to reach US$ 74.31 million by 2027 from US$ 19.57 million in 2020; it is estimated to grow at a CAGR of 20.3% from 2021 to 2027.
Increasing Drug Launches and Robust Pipeline can be a major driver for the market
Drug launches will help to differentiate their drug through messaging, post-launch data and services and with that broad customer advocacy via a superior customer experience will also be there. This will help the world to gain as much as information they need.
COVID-19 Poses Great Challenges for Global Netherton Syndrome Market The pandemic has prompted a need to re-assess the syndrome through various campaigns physically and socially. Through which world is getting more aware through such mediums and are able to overcome their syndrome. At present, while the world is going through with a health hazard, this is the most significant opportunity to recognize the prospects of a truly digital society globally, helping in sharing sporadic information, innovations and technologies between communities and governments.
Regional Analysis
The Global Netherton syndrome market is segmented into North America, Asia-Pacific, Europe, Middle-East & Africa and Latin America. APAC is considered to be the largest share in the market where as Europe is predicted to play smaller share in the market.
Key Players
The global market key players includes Lifemax Laboratories, Inc.; Azitra, Inc.; Sixera Pharma Ab; Dermelix Biotherapeutics; Matrisys Bioscience; Quoin Pharmaceuticals Ltd.; and Krystal Biotech, Inc.
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