Scrip is part of the Business Intelligence Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC’s registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

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


BMS/Pfizer gain FDA nod for Eliquis in 2012, after all

This article was originally published in Scrip

Executive Summary

With the US FDA's decision on Bristol-Myers Squibb's and Pfizer's anticoagulant Eliquis (apixaban) not expected until 17 March, the companies' notice they would not provide detailed information on the 28 December approval until the following week might be a hint that even they were caught off guard by the early verdict – even though it was the second go-around for the drug's application at the agency.



Related Companies




Ask The Analyst

Please Note: Click here for more information on the Ask the Analyst service.

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