Futibatinib receives Breakthrough Designation from FDA for advanced cholangiocarcinoma

Share on facebook
Share on twitter
Share on linkedin
Share on email
Share on print

Futibatinib (TAS-120), a covalently-binding FGFR inhibitor, has received Breakthrough Therapy designation from FDA for patients with previously treated locally advanced or metastatic cholangiocarcinoma harboring FGFR2 gene rearrangements, including gene fusions.

To access this subscriber-only content please log in or renew your subscription.

Looking for IP Login? Our IP Login system is now automatic. If your institution has a site license, please log in from on site or via your VPN to access this content.

Login Subscribe
Table of Contents

YOU MAY BE INTERESTED IN

Login