Video
Dr. Allen Discusses CO-1686 as a Treatment for Lung Cancer
Author(s):
Andrew R. Allen, BM, BCh, MA, MRCP, PhD, Executive Vice President of Clinical and Pre-Clinical Development, Chief Medical Officer, Co-Founder, Clovis Oncology, provides an overview of CO-1686.
Andrew R. Allen, BM, BCh, MA, MRCP, PhD, Executive Vice President of Clinical and Pre-Clinical Development, Chief Medical Officer, Co-Founder, Clovis Oncology, provides an overview of CO-1686.
Over the past 10 years, oncologists have been able to use first-generation EGFR inhibitors to treat patients with EGFR-positive lung cancer. However, patients will eventually develop acquired resistance to these agents through a second mutation in EGFR known as T790M.
Allen says Clovis has developed CO-1686 to inhibit T790M as well as the activating mutations in EGFR while sparing the inhibition of the normal, or wild-type, EGFR.
Data for CO-1686 were first presented at ASCO in 2013 with a follow-up this year. Prior to the 2014 ASCO Annual Meeting, CO-1686 was granted a breakthrough therapy designation from the FDA.
Allen says data on CO-1686 presented at the 2014 ASCO Annual meeting showed that patients with confirmed T790M mutations saw a 60% objective response rate when treated with CO-1686 alone. The median progression-free survival has not yet been reached, Allen says, but the current estimate exceeds 12 months.
