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's NME Approval Rebound At Risk: Drought Of Novel Products In Line For Action In Remainder Of 2010 Could Depress Upward Trend From First Half

Executive Summary

Almost one-third fewer novel product applications are on FDA's user fee calendar for the second half of 2010 as compared to the docket at the same point in 2009, a dearth that could imperil the slow but steady improvement in annual new molecular entity and novel biologic approvals after the nadirs reached earlier in the decade

You may also be interested in...



Chart: New Molecular Entities Approved In The First Half Of 2010

New Molecular Entities Approved In The First Half Of 2010

FDA Says Lux's Uveitis Treatment Luveniq Needs Another Clinical Trial

In a "complete response" letter following the last-minute cancellation of an advisory committee review in June, FDA asks the biotech to do an additional confirmatory study.

FDA Panel Backs Broad Acute Coronary Syndromes Claim For Brilinta

An FDA advisory committee's blessing of AstraZeneca's Brilinta clinical strategy should reassure other drug developers that a single pivotal trial encompassing the spectrum of acute coronary syndromes and treatment strategies can support a broad claim for reducing thrombotic events

Related Content

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS052531

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