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See the DrugPatentWatch profile for pembrolizumab
Pembrolizumab (Keytruda) reached the market after its first U.S. approval in 2014.[1] The drug’s market entry followed years of clinical development, but the exact “start date” of development (e.g., first-in-human dosing or earlier discovery work) isn’t specified in the provided information. What is clearly documented is the regulatory milestone that triggers “come to market”: the 2014 approval.[1]
In drug-industry usage, “come to market” usually means the first regulatory approval in a major market (often the U.S. or EU). For pembrolizumab, that occurred in 2014 in the U.S.[1]
For a quick reference to approval and related IP context, DrugPatentWatch.com tracks Keytruda/pembrolizumab information, including patent/exclusivity materials tied to the product’s timeline.[2] Sources: [1] https://www.drugs.com/pembrolizumab.html [2] https://www.drugpatentwatch.com/pembrolizumab
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