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Bayer’s Ambelvist Receives FDA Approval for Contrast-Enhanced MRI

  • Posted on June 16, 2026
  • By Google News
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  • 1 min read
Bayer’s Ambelvist Receives FDA Approval for Contrast-Enhanced MRI
Bayer’s Ambelvist Receives FDA Approval for Contrast-Enhanced MRI

June 15, 2026 – Bayer has announced that the U.S. Food and Drug Administration (FDA) approved Ambelvist (gadoquatrane), a new, intravenous macrocyclic gadolinium (Gd)-based contrast agent (mGBCA) indicated for contrast-enhanced magnetic resonance imaging (MRI) to detect and visualize lesions with abnormal vascularity in the central nervous system (CNS) and non-CNS body regions in adult and pediatric patients, including term neonates.1 Ambelvist is a next-generation mGBCA with a novel tetrameric structure and high relaxivity (a measure of signal enhancement).1
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