Logo

Abbott's XIENCE Stent Receives the US FDA's Approval for Shortest Blood Thinner Course in Patients with High Bleeding Risk

Share this

Abbott's XIENCE Stent Receives the US FDA's Approval for Shortest Blood Thinner Course in Patients with High Bleeding Risk

Shots:

  • Abbott has received approval in the US & and CE mark for XIENCE stents- the shortest approved DAPT labeling as short as 28 days in patients with high bleeding risk. XIENCE Skypoint stent also received FDA approval in the US and CE Mark in the EU
  • Additionally- patients with stents are typically on DAPT regimens (aspirin and P2Y12 inhibitors) for 6 -12mos. to prevent blood clots from blocking the stented vessel
  • Abbott's XIENCE 28 and XIENCE 904 studies showed that DAPT can be safely discontinued early as short as 28 days with no increased risk in patients’ AEs

  | Ref: Abbott | Image: Medical Device and Diagnostic Industry

Click here to­ read the full press release 

Senior Editor

This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

Share this article on WhatsApp, LinkedIn and Twitter

Join the PharmaShots family of 12000+ subscribers

I accept the Terms and Conditions