Pink Sheet 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

Bristol/Pfizer's Apixaban Gets A Chance At The Inside Track

This article was originally published in The Pink Sheet Daily

Executive Summary

FDA has agreed to review the anticoagulant based on the results of the AVERROES trial, offering a potentially faster route to market.

You may also be interested in...



Bristol R&D Update: Apixaban Filing Delayed, Ipilimumab Approval Expected

Contrary to expectations, Bristol-Myers Squibb will not file early for a narrow indication of the novel anticoagulant apixaban.

Bristol R&D Update: Apixaban Filing Delayed, Ipilimumab Approval Expected

Contrary to expectations, Bristol-Myers Squibb will not file early for a narrow indication of the novel anticoagulant apixaban.

Xarelto Back On Track: J&J Answers "Complete Response" Letter And Files For Atrial Fibrillation

Simultaneously, partner Bayer submits applications in Europe, where rivaroxaban already is approved, for those indications and one more.

Related Content

Topics

Latest News
See All
UsernamePublicRestriction

Register

PS071357

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