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NeoGenomics Launches FDA-Approved PTEN IHC Companion Diagnostic for Prostate Cancer

Healthcare & BiotechTechnology & InnovationProduct LaunchesRegulation & Legislation

NeoGenomics launched PTEN IHC CDx, described as the first IHC companion diagnostic test approved by the U.S. FDA for patients with prostate adenocarcinoma. The FDA approval and product debut are a meaningful regulatory milestone that could support adoption in prostate cancer diagnostics.

Analysis

NeoGenomics launched PTEN IHC CDx, described as the first IHC companion diagnostic test approved by the U.S. FDA for patients with prostate adenocarcinoma. The FDA approval and product debut are a meaningful regulatory milestone that could support adoption in prostate cancer diagnostics.

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