Tests found that the foreign matter does not pose a clinical risk to patients.
"Cause temporary or medically reversible adverse health consequences." ...
Amgen recalls 934K bottles of Corlanor and Sensipar due to foreign material and manufacturing deviations, per FDA June 23 report.
The tablets involved in the recall were distributed in the U.S. from Oct. 28, 2021, to Dec. 30, 2025 ...
Amgen has declined a request from the FDA to voluntarily withdraw Tavneos from the U.S. market. The FDA on Jan. 16 cited concerns about ChemoCentryx’s process for re-adjudicating primary endpoint ...
The FINANCIAL — Amgen on June 18 announced that a Phase 3 study evaluating Vectibix (panitumumab) and best supportive care (BSC) met its primary endpoint, demonstrating a statistically significant ...
The FINANCIAL — Amgen on July 31 announced the submission of a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug Administration (FDA) for Prolia (denosumab) for the treatment ...