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September 15, 2026

FDA reduces monitoring time for Amgen’s Imdelltra infusions

The US Food and Drug Administration (FDA) has approved an update to the prescribing information for Amgen’s Imdelltra (tarlatamab-dlle), reducing the recommended monitoring time for patients with extensive-stage small cell lung cancer (ES-SCLC) after their first two infusions.

FDA reduces monitoring time for Amgen’s Imdelltra infusions