Eli Lilly has earned FDA approval for its Cyramza in liver cancer patients, the first biomarker-driven therapy of its kind, the Indianapolis-based drugmaker announced.
Cyramza (ramucirumab injection) is approved for patients with hepatocellular carcinoma who have an alpha-fetoprotein level at or below 400 ng per ml and who have already been treated with sorafenib. AFP is a biomarker that can be assessed through a blood tests, which Lilly officials say makes it much easier to determine treatment options for patients.
The approval comes after Lilly handed up results from the Phase III REACH-2 study which selected patients based on their AFP levels. Cyramza was previously approved, singly or in combination, for gastric, non-small cell lung, colorectal and hepatocellular cancers.
