FDA approves drug for treatment-resistant metastatic colorectal cancer

The FDA has approved the use of tucatinib — a drug engineered by biotech company Seagen — in tandem with trastuzumab as a second-line treatment for colorectal cancer that has not responded to other therapies.

Advertisement

The drug was approved under the FDA’s Accelerated Approval Program based on the treatment success rate in previous clinical trials, according to a Jan. 19 news release from the company. 

 

“Historically, patients with HER2-positive metastatic colorectal cancer who have progressed following front-line therapy have had poor outcomes,” John Strickler, MD, an associate professor at Duke University Medical Center and lead investigator during clinical trials of the drug, said in the release. “The FDA approval of a chemotherapy-free combination regimen that specifically targets HER2 is great news for these patients.”

 

At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.

Advertisement

Next Up in GI & Endoscopy

Advertisement

Comments are closed.