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See the DrugPatentWatch profile for Pylarify
Pylarify (piflufolastat F 18) received its European Union approval on 7 November 2023 [1].
Pylarify is a radiopharmaceutical used for positron emission tomography (PET) imaging. In the EU, it is indicated for detection of prostate-specific membrane antigen (PSMA)-positive lesions in patients with prostate cancer when appropriate for clinical management (based on the EU label) [1].
The EU approval date is published by the European Medicines Agency (EMA) and is linked to the marketing authorisation for Pylarify [1]. Sources: [1] https://www.ema.europa.eu/en/medicines/human/EPAR/pylarify
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