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

Unresolved Review Issues: Clinical Trials Are Easier Fix Than Safety, Efficacy

Executive Summary

Problems with clinical trial design and/or execution identified pre-submission are the issues most likely to be resolved in advance of first FDA action, Booz Allen Hamilton's first-cycle review report finds

You may also be interested in...



Yentreve NDA withdrawal (correction)

Lilly maintains that a QT prolongation signal was not a factor in the firm's decision to withdraw its application for the stress urinary incontinence therapy Yentreve (duloxetine), as suggested in a 1story in the Feb. 27 issue of "The Pink Sheet" regarding Booz Allen's first-cycle review report. According to review documents for duloxetine in treatment of depression, approved under the trade name Cymbalta, FDA's Division of Reproductive & Urologic Drug Products was concerned that duloxetine may have the potential to prolong the QT interval in patients receiving CYP2D6 and CYP1A2 inhibitors. The division felt the issue needed to be addressed pre-approval due to the common use of CYP2D6 and CYP1A2 inhibitors in the SUI population. Lilly says the withdrawal was due to Yentreve's risk/benefit ratio...

Yentreve NDA withdrawal (correction)

Lilly maintains that a QT prolongation signal was not a factor in the firm's decision to withdraw its application for the stress urinary incontinence therapy Yentreve (duloxetine), as suggested in a 1story in the Feb. 27 issue of "The Pink Sheet" regarding Booz Allen's first-cycle review report. According to review documents for duloxetine in treatment of depression, approved under the trade name Cymbalta, FDA's Division of Reproductive & Urologic Drug Products was concerned that duloxetine may have the potential to prolong the QT interval in patients receiving CYP2D6 and CYP1A2 inhibitors. The division felt the issue needed to be addressed pre-approval due to the common use of CYP2D6 and CYP1A2 inhibitors in the SUI population. Lilly says the withdrawal was due to Yentreve's risk/benefit ratio...

Mid-Phase III Meetings Suggested As Way To Increase First-Cycle Approvals

FDA should consider conducting mid-Phase III meetings with drug sponsors as a way to improve the likelihood of approving an application during the first review cycle, a report by Booz Allen Hamilton recommends

Related Content

Latest Headlines
See All
UsernamePublicRestriction

Register

PS046925

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