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

FDA Postpones PDUFA Date For Schering-Plough’s Bridion To Third Quarter

This article was originally published in The Pink Sheet Daily

Executive Summary

Agency requires more time to analyze hypersensitivity study, firm says.

You may also be interested in...



Schering Plough’s Bridion Faces FDA Setback

Safety concerns render anesthesia injection “not approvable” in U.S.

Schering Plough’s Bridion Faces FDA Setback

Safety concerns render anesthesia injection “not approvable” in U.S.

Europe Likes Schering’s Bridion, But Not Takeda’s Rozerem

New opinion includes CHMP skepticism of insomnia drug.

Related Content

Topics

Latest News
See All
UsernamePublicRestriction

Register

PS067434

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