GSK plc GSK announced that the FDA accepted its biologics license application (BLA) seeking approval for the Blenrep ...
Findings from a phase 3 trial with Blenrep, Velcade and dexamethasone in relapsed/refractory multiple myeloma will be ...
The DREAMM-7 trial showed Blenrep with BorDex lowered death risk in relapsed/refractory multiple myeloma vs. standard ...
GSK is carving out a niche for Blenrep in the second-line multiple myeloma setting, for which it projects multi-blockbuster ...
The US Food and Drug Administration (FDA) is expected to make a Prescription Drug User Fee Act (PDUFA) decision by mid-2025.
GSK (GSK) announced the US Food and Drug Administration, FDA, has accepted for review a Biologics License Application, BLA, for Blenrep in combinations with bortezomib plus dexamethasone and ...
GSK plc (GSK, GSK.L) announced that the US Food and Drug Administration has accepted for review a Biologics License Application (BLA) ...
在抗肿瘤药物研发的复杂舞台上,Blenrep的故事宛如一出跌宕起伏的戏剧。曾几何时,这款靶向BCMA的抗体药物被视为GSK重返癌症领域的利器,然而,市场的残酷和临床试验的不确定性让它经历了一波三折的命运。对于许多人来说,Blenrep的退市似乎意味着它的终章,但就在GSK即将放弃时,新的希望又重新燃起。在临床试验DREAMM-7的中期分析显示出积极结果时,这款产品又重新回到了公众的视野中。
第15届医博会期间,同写意生物医药新基建链盟将举办ADC专场,邀请抗体/ADC研发端、生产端和供应链端的企业负责人与会深度交流,帮助行业优化和提升生物药创新生态链。
The FDA has approved GlaxoSmithKline’s multiple myeloma drug Blenrep, a first-in-class potential blockbuster that will be used in advanced disease. Blenrep (belantamab mafodotin) has been ...