Lantheus Shares Trading Higher On FDA Approval For Imaging Agent For Identification Of Prostate Cancer

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  • The FDA has approved Lantheus Holdings Inc's LNTH Pylarify, a positron emission tomography (PET) imaging agent, to identify suspected metastasis or recurrence of prostate cancer.
  • Pylarify is an F 18-labeled prostate-specific membrane antigen (PSMA) imaging agent for diagnosing prostate cancer. It is the first and only commercially available approved PSMA PET imaging agent for prostate cancer, said the company.
  • The product will be immediately available in parts of the mid-Atlantic and southern regions, and availability is expected to expand over the next six months, with broad availability across the U.S. anticipated by the end of 2021.
  • Pylarify was developed to target PSMA, a protein overexpressed on the surface of more than 90% of primary and metastatic prostate cancer cells.
  • It binds to the target, enabling the reader of the PET scan to detect and locate the disease.
  • Price Action: LNTH shares are up 15.3% at $22.49 during the premarket session on the last check Thursday.
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Posted In: BiotechNewsHealth CareSmall CapFDAGeneralBriefsprostate cancer
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