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Lantheus receives FDA approval of Pylarify injection, the first and only commercially available PSMA PET imaging agent for prostate cancer.

Read time: 1 mins
Last updated:1st Jun 2021
Published:30th May 2021
Lantheus Holdings, Inc. announced that the FDA has approved Pylarify, an F 18-labeled prostate-specific membrane antigen (PSMA) targeted positron emission tomography (PET) imaging agent to identify suspected metastasis or recurrence of prostate cancer.
Condition: Imaging:PET
Type: drug
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