Macular Degeneration is an indication for drug development with over 570 pipeline drugs currently active. According to GlobalData, preregistered drugs for Macular Degeneration have a 80% likelihood of approval (LoA) indication benchmark. GlobalData’s report assesses how phase transition success rate (PTSR) and likelihood of approval (LoA) scores for pipeline drugs in Macular Degeneration compared to historical benchmarks. Buy the report here.
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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Macular Degeneration overview
Macular degeneration is primarily an age-related retinal condition. There are two types of macular degeneration — wet AMD and dry AMD. Genetics and environmental factors like smoking, obesity, diet, family genes can cause MD. Symptoms include visual distortions, reduced central vision, difficulty adapting to low light, blurry or fuzzy vision. Treatment include Syfovre and anti-VEGF drugs such as avastin (bevacizumab), lucentis (ranibizumab), eylea (aflibercept). Vitamins A, C, and E are the most effective vitamins for reducing the risk of macular degeneration.
For a complete picture of PTSR and LoA scores for drugs in Macular Degeneration, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
