Taiho's Lonsurf combo notches up another approval for mCRC
The US Food and Drug Administration (FDA) has approved Lonsurf (trifluridine/tipiracil), developed by Taiho Oncology Inc and Taiho Pharmaceutical, subsidiaries of Japanese drugmaker Otsuka Holdings (TYO: 4578), with the decision coming ahead of the August 13 expected date.
Lonsurf is now authorized as a single agent or in combination with bevacizumab for the treatment of adult patients with metastatic colorectal cancer (mCRC) previously treated with fluoropyrimidine-, oxaliplatin-, and irinotecan-based chemotherapy, an anti-VEGF biological therapy, and if RAS wild-type, an anti-EGFR therapy.
Just a couple of days ago, Taiho’s French partner Servier gained approval for this combination for mCRC from the European Commission.
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