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

Genentech/Curis Hedgehog Inhibitor Gets Unclear Results In Ovarian Cancer Maintenance Study

This article was originally published in Pharmaceutical Approvals Monthly

Executive Summary

Roche/Genentech will "make a portfolio decision" on development of the novel Hedgehog inhibitor GDC-0449 in advanced ovarian cancer after further analyses of Phase II data, partner Curis said Aug. 9. Early analyses of top-line data "warrant additional investigation to clarify and interpret potential clinical activity," the company said

You may also be interested in...



Hedgehog stumbles in clinical trial

Curis' first-in-class Hedgehog pathway inhibitor GDC-0449 failed in a Phase II clinical trial in metastatic colorectal cancer, where it was studied in combination with partner Roche/Genentech's Avastin and FOLFOX or FOLFIRI chemotherapy, the firms announced June 16. The trial did not meet the primary endpoint of extending time from randomization to disease progression or death in patients getting the GDC-0449 combination versus the standard of care arm. Curis is confident that other trials will bear out the Hedgehog inhibitor's potential, because the pathway is thought to act by different mechanisms in other tumor types; the firm noted that proof of concept has been achieved in advanced basal cell carcinoma, which is "almost always" the result of a specific mutation in a component of the Hedgehog pathway. Roche already has a pivotal Phase II of GDC-0449 underway in advanced basal cell carcinoma and the firm has indicated it expects to initiate a Phase II in operable basal cell carcinoma during the second half of 2010. Results are also expected in the second half from a randomized Phase II in advanced ovarian cancer in a maintenance setting, "which is evaluating the ability of GDC-0449 to slow the time to recurrence in patients ... in complete remission, by impeding the residual cancer cell's ability to grow," Curis said

FDA Priority Review Voucher Redemption Fee Set At $4.6 Million In FY 2011

Redeeming a priority review voucher obtained by developing a drug for a tropical disease will cost companies $6.1 million in fiscal 2011

September 2010 Approvals

Product

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS004523

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