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Polarean’s Xenoview (xenon Xe 129 hyperpolarized) Receives the US FDA’s Approval for Lung Ventilation

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Polarean’s Xenoview (xenon Xe 129 hyperpolarized) Receives the US FDA’s Approval for Lung Ventilation

Shots:

  • The US FDA has approved Xenoview, a hyperpolarized contrast agent indicated for use with MRI for lung ventilation in adults & pediatric patients aged ≥12yrs. The product is administered by oral inhalation as a single 10-15 second breath hold MRI procedure
  • The approval was based on the P-III trial (Study 1 & 2) evaluating Xenoview MRI vs xenon Xe 133 scintigraphy in 80 patients. (Study 1) patients evaluated for lung resection surgery & in (Study 2) for lung transplant surgery
  • Both the trial met their 1EPs i.e., the (Study 1 &2) trial results showed observed estimation of 1.4% & 1.6% for the mean within-patient difference was within a predetermined equivalence interval in the postoperative percentage of remaining & overall lung ventilation b/w  Xenoview & xenon Xe 133 imaging

Ref: Globenewswire | Image: Polarean

Related News:- Polarean Reports the NDA Submission of Hyperpolarised 129Xenon Gas Drug-Device Diagnostic to the US FDA for Lung Imaging

Click here to­ read the full press release 

Senior Editor

Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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