5 天
环球老虎财经 on MSN强生放弃“达雷妥尤单抗升级版”!HexaBody-CD38临床折戟,Genmab股价 ...3月10日,Genmab宣布强生决定不再行使HexaBody-CD38(GEN3014)的全球开发和商业化选择权。消息出来后,Genmab股价下跌7.8%。 截图来源:企业官网 ...
为解决皮肤 T 细胞淋巴瘤(CTCL)治疗难题,研究人员探究 CD38 作用及联合疗法,发现联合治疗可提升疗效。 皮肤 T 细胞淋巴瘤(Cutaneous T-Cell Lymphoma,CTCL)是一种让人头疼的非霍奇金淋巴瘤,它专门 “攻击” 皮肤里的恶性 T 细胞。得了这种病,患者皮肤状况 ...
is a CD38 monoclonal antibody that binds to a specific epitope on the CD38 receptor on MM cells, inducing distinct antitumor activity. It is designed to work through multiple mechanisms of action ...
来自MSN2 个月
新星崛起,强生遇劲敌!多发性骨髓瘤药物市场竞争格局分析一、CD38单抗市场竞争分析 1. 达雷妥尤 ... 3-5分钟皮下给药将大幅缩短MM和AL患者的治疗时间,让中国的浆细胞疾病的治疗实现了和国际接轨。
Sarclisa is a CD38 monoclonal antibody that targets the CD38 receptor on MM cells, inducing apoptosis and immunomodulatory activity. In December 2023, Sanofi reported that its Phase III IMROZ ...
(RTTNews) - Genmab A/S (GMAB) Monday announced that Johnson & Johnson (JNJ) has decided not to exercise its option to develop and commercialize HexaBody-CD38 for multiple myeloma, for a worldwide ...
Johnson & Johnson is dropping a partnership with Genmab centered around a CD38 monoclonal antibody, prompting the latter company to discontinue development of the program. Back in 2019 ...
MM continues to be a therapeutically challenging ... but not limited to, mAbs specific for CD38, CS1, CD40, CD74, CD70, HM1.24, IL-6 and B2MG directed against a number of potential targets for ...
While the initial HexaBody-CD38 clinical data is promising and showed robust clinical efficacy, following a thorough evaluation of the data, the market landscape, and Genmab’s rigorous portfolio ...
Johnson & Johnson has decided that it will not exercise its option to receive a worldwide license to develop, manufacture and commercialize HexaBody-CD38 Genmab will not pursue further clinical ...
Despite initial clinical data showing efficacy, Genmab has decided to discontinue further clinical development of HexaBody-CD38. “While we are disappointed that J&J has decided not to advance ...
Johnson & Johnson has decided that it will not exercise its option to receive a worldwide license to develop, manufacture and commercialize HexaBody-CD38 Genmab will not pursue further clinical ...
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