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With priority review, J&J/Bayer take step closer to third Xarelto indication

This article was originally published in Scrip

Executive Summary

Bayer HealthCare and Johnson & Johnson said they were granted a six-month priority review by the US FDA on the firms' supplemental new drug application (sNDA) for their oral anticoagulant Xarelto (rivaroxaban) as a therapy to reduce the risk of thrombotic events in patients with acute coronary syndrome (ACS).





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