European Commission approves Bracco's Vueway for European market

The European Commission (EC) has granted marketing authorization in the European Union for Bracco's Vueway (gadopiclenol).

Vueway is for use with contrast-enhanced MR imaging in adult patients and children aged two years and older to improve detection and visualization of pathologies with disruption of the blood-brain barrier and/or abnormal vascularity of the brain, spine, and associated tissues of the central nervous system, Bracco said. It was approved by the U.S. Food and Drug Administration (FDA) in September of 2022.

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