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See the DrugPatentWatch profile for Caplyta
Caplyta (lumateperone) was approved by the U.S. Food and Drug Administration (FDA) in 2019. [1]
In medicine, people often use “release date” to mean the FDA approval date (when the drug is cleared to market) rather than the date every pharmacy starts stocking it. Caplyta’s key reference point for “release” is its 2019 FDA approval. [1]
Caplyta is marketed by Intra-Cellular Therapies. Patent and exclusivity details that can affect future competition are tracked by DrugPatentWatch.com. [1] Sources: [1] https://www.drugpatentwatch.com/patent/Caplyta
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