FDA Panel Votes to Defer Decision on Retifanlimab for Anal Cancer Retifanlimab is an investigational intravenous PD-1 inhibitor. (Credit: Getty Images.)
The Food and Drug Administration (FDA)âs Oncologic Drugs Advisory Committee (ODAC) voted 13 to 4 to defer a regulatory decision on retifanlimab, an investigational PD-1 inhibitor for locally advanced or metastatic squamous cell carcinoma of the anal canal (SCAC), until further data from a confirmatory trial are made available.
The Biologics License Application (BLA) submission for retifanlimab included data from an open-label, single-arm phase 2 trial (POD1UM-202; ClinicalTrials.gov Identifier: NCT03597295), which evaluated retifanlimab in 94 adults with locally advanced or metastatic SCAC who progressed after platinum-based chemotherapy.
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