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如果獲得批準，Tisotumab Vedotin將成為首個獲得歐盟上市許可的用於治療宮頸癌患者的ADC。丹麥生物技術公司<光算谷歌seostrong>光算蜘蛛池Genmab和輝瑞公司宣布，歐洲藥品管理局（EMA）已批準審查抗體偶聯藥物（ADC）Tisotumab Vedotin的上市許可申請（MAA）。2月2日 ， |
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