Pink Sheet is part 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

UsernamePublicRestriction
UsernamePublicRestriction

New PARP On The Block: BioMarin Starts Phase III, Could Prove To Be Best-In-Class

This article was originally published in Pharmaceutical Approvals Monthly

Executive Summary

Class’s comeback gets more fuel at AACR/NCI/EORTC targeted therapies meeting. Evidence indicates BioMarin may have the most powerful PARP inhibitor, though AstraZeneca and Tesaro are slightly further in development.

You may also be interested in...



Tesaro’s Niraparib Takes PARP Inhibitor Lead In Ovarian Cancer

Tesaro Inc. announced the launch of a Phase III trial for its PARP inhibitor niraparib in ovarian cancer, while registrational data from three global Phase III studies for anti-emetic rolapitant are due by the end of 2013.

Pharma Adapts Ovarian Cancer Drugs Amid Genomics Revolution

Astra Zeneca hustles on genomic analyses of PARP inhibitor olaparib after drug fails to improve overall survival in a Phase II ovarian cancre trial, which could signify a revival. Meanwhile, Avastin lead investigator defends anti-angiogenesis approach, considering tremendous diversity of the relatively uncommon disease.

Topics

Related Companies

UsernamePublicRestriction

Register

PS005284

Ask The Analyst

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

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