abbvie gk (headquarters: minato-ku, tokyo; president: james feliciano, hereafter “abbvie”) and eisai co., ltd. (headquarters: tokyo; ceo: haruo naito, hereafter “eisai”) today announced an approval of additional indication of humira® (generic name: adalimumab [recombinant], hereafter “humira”), a fully human anti-tnfα monoclonal antibody, for the treatment of pyoderma gangrenosum (hereafter “pg”). humira was granted orphan drug designation for the treatment of pg in 2019. this indication counts for humira’s 12th indication in japan and makes humira the world’s first drug indicated for the treatment of pg.
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