eisai co., ltd. (headquarters: tokyo, ceo: haruo naito, “eisai”) announced today that the results of an interim analysis of a phase ib/ii clinical study (study 218) of its in-house discovered and developed anticancer agent eribulin mesylate (halichondrin class microtubule dynamics inhibitor, product name: halaven®, “eribulin”) in combination with the anti-pd-1 antibody pembrolizumab developed by merck & co., inc., kenilworth, nj, usa (known as msd outside the u.s. and canada), in patients with metastatic triple-negative breast cancer have been presented at the 39th annual san antonio breast cancer symposium held from december 6 to 10, 2016. development of this combination regimen is being conducted jointly under the cooperation of both companies.
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