18Feb/13

Novartis' Zortress cleared by FDA for liver transplants – PMLiVE

Novartis’ Zortress cleared by FDA for liver transplants
PMLiVE
Zortress (everolimus) is already approved in the US for preventing organ rejection in kidney transplant patients, and was cleared for the liver transplant indication last year in Europe, where it is sold as Certican and also used in renal and heart
US FDA approves Novartis’ Zortress to prevent organ rejection in adult liver pharmabiz.com
FDA grants fresh approval for Novartis’ ZortressPharmaTimes
Novartis Zortress medication wins FDA nod to prevent liver transplantation Pharmaceutical Business Review

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16Feb/13

NOVARTIS AG : Novartis drug Zortress® is first in over a decade approved by … – 4-traders (press release)

NOVARTIS AG : Novartis drug Zortress® is first in over a decade approved by
4-traders (press release)
Basel, February 15, 2013 – Novartis announced today that the US Food and Drug Administration (FDA) has approved Zortress® (everolimus) for the prophylaxis of organ rejection in adult patients receiving a liver transplant. Zortress is the first
FDA Nod For Novartis Drug To Avert Organ Failure In Liver TransplantRTT News
US FDA okays Novartis drug to prevent liver transplant rejectionReuters

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13Feb/13

Boston's Promus PREMIER Everolimus-Eluting PtCr stent system receives CE … – pharmabiz.com


Platinum today

Boston’s Promus PREMIER Everolimus-Eluting PtCr stent system receives CE
pharmabiz.com
Boston Scientific Corporation, a worldwide developer, manufacturer and marketer of medical devices, has received CE Mark approval for the Promus PREMIER Everolimus-Eluting Platinum Chromium Coronary Stent System, the company’s next-generation
CE Mark for BSX’s Promus Premier – Analyst BlogInvestorIdeas.com (press release)
Promus Premier platinum stent wins CE Mark approvalPlatinum today

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