Press release
Increasing adoption of the Alternatives for the Therapeutics of vision in patients to bring profitable opportunities for the Stargardt Disease market
Stargardt disease also called Stargardt's macular dystrophy (SMD) that affects approximately one in 10,000 people and described as central vision loss early in life. Stargardt Disease is most commonly caused by mutations in the ABCA4 gene located on chromosome 1 and is inherited in an autosomal recessive manner. This disorder affects the specialized light-sensitive tissue present in the retina. This type of macular degeneration affects the center of the retina which is known as macula which adds sharpness to the central vision. The affected individuals also show the symptoms of color blindness. The signs and symptoms appear in late childhood which is responsible for disease progression.Request Free Sample Report of Stargardt Disease Therapeutics Market Report @
https://www.coherentmarketinsights.com/insight/request-sample/1314
Impact of Coronavirus (COVID-19) Pandemic on Clinical Trials and Drug Development
The COVID-19 pandemic caused major disruptions to clinical trial execution in the U.S., impacting key stakeholders across the industry. Investigative site capabilities experienced upheaval, driven by staff furloughs, social-distancing protocols, financial losses, and concerns over patient safety. Sponsors, CROs, and other organizations that support drug development shifted to remote working environments. An estimated 80% of non-COVID-19 trials were stopped or interrupted as a result of the COVID-19 pandemic.
An April 2020 study suggests that investigative sites demonstrated flexibility and ingenuity in adopting new approaches in order to cope with challenges presented by the COVID, with over half of investigative sites transitioning to virtual approaches to interact with patients. More recently, follow-up studies performed in August 2020 have identified persistent impact of COVID, with over 60% reporting an 'average' or greater level of impact on ongoing trials and initiation of new trials. Respondents specifically highlighted challenges in patient enrollment and recruitment.
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๐ ๐ฅ๐๐ญ ๐๐ง๐ฌ๐ญ๐๐ง๐ญ ๐๐ข๐ฌ๐๐จ๐ฎ๐ง๐ญ ๐จ๐ ๐๐$ ๐๐๐๐
๐๐ฎ๐ฒ ๐๐ก๐ข๐ฌ ๐๐จ๐ฆ๐ฉ๐ฅ๐๐ญ๐ ๐ ๐๐ฎ๐ฌ๐ข๐ง๐๐ฌ๐ฌ ๐๐๐ฉ๐จ๐ซ๐ญ:
https://www.coherentMarketinsights.com/promo/buynow/1314
Major Market Competitors: Kubota Pharmaceutical Holdings Co., Ltd., Stargazer Pharmaceuticals Inc, Iveric Bio, Inc., Sanofi S.A., Alkeus Pharmaceuticals Inc., Astellas Pharma Inc., CHABiotech CO., Ltd., ReVision Therapeutics, Inc., Lin BioScience, Inc., Biogen Inc., F. Hoffmann-La Roche AG
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Stargardt disease, the most common form of inherited juvenile macular degeneration, is caused by mutations in the ABCA4 gene. It typically manifests in late childhood or adolescence, leading to progressive central vision loss. With an estimated prevalence of 1 in 8,000 to 10,000 individuals worldwide, Stargardt disease is classified as a rare genetic disorder but represents a significant unmet need within ophthalmology.
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