Medtech Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

Ev3's Pipeline

This article was originally published in The Gray Sheet

Executive Summary

FDA formally accepts ev3's PMA application for its Pipeline embolization device to treat "large, giant and wide-necked" cerebral aneurysms, the firm announces June 21. The PMA, submitted May 18, also has been granted expedited review by FDA, ev3 said. The agency grants expedited review - placing the PMA at the head of the pre-market review queue - if the device treats or diagnoses a life-threatening or irreversibly debilitating condition, and addresses an unmet medical need, according to FDA. "Safe and effective treatment of large and giant, wide-neck or non-saccular aneurysms remains a significant unmet clinical need," according to the company. Ev3 previously said it anticipates an FDA advisory panel review later this year and U.S. approval in 2011 (1"The Gray Sheet" May 24, 2010). Covidien will acquire ev3 for $2.6 billion under a June 1 agreement (2"The Gray Sheet" June 7, 2010)

You may also be interested in...



Covidien Makes Big Play In Endovascular With $2.6 Billion ev3 Deal

Covidien says its large international operations will further accelerate ev3's fast-growing neurovascular and peripheral vascular businesses following its planned $2.6 billion acquisition of the endovascular firm

New Products In Brief

Ev3's Pipeline: Firm completes modular PMA application for its Pipeline embolization device to treat uncoilable or failed aneurysms, announced May 18. Ev3 says it anticipates an FDA advisory panel review of the endovascular treatment "sometime later in the year" and U.S. approval in 2011. Ev3 acquired the self-expanding cylindrical mesh implant through its purchase of Chestnut Medical Technologies in 2009 (1"The Gray Sheet" June 8, 2009)

Chinese Firms Up Their Game In Novel Flu Antiviral Development

Joincare Pharmaceutical and partner TaiGen Biotechnology tout preliminary Phase III results in uncomplicated acute influenza for TG-1000, a homegrown follower of Shionogi/Roche’s oral antiviral Xofluza. Novel antivirals for flu were hotly pursued by Chinese developers throughout 2023.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

MT029051

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel