A Chinese Phase III study has met its primary endpoint in significantly increasing progression-free survival (PFS) in bowel cancer patients treated with Erbitux (cetuximab) plus Folfox chemotherapy, compared with the latter alone.
German's Merck KGaA welcomed the results of the Tailor study, supporting other evidence it has provided of its Erbitux antibody in combination with Folfox as a standard first-line treatment for patients with RAS wild-type metastatic colorectal cancer (mCRC).
Erbitux has already obtained market authorization in over 90 countries worldwide for colorectal cancer and Merck KGaA will work with relevant authorities to make it available for patients in China as a first-line treatment as soon as possible.
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