Amneal announced FDA acceptance of its Biologics License Application (BLA) for two proposed denosumab biosimilars ...
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长期使用糖皮质激素会对骨骼健康产生显著影响,其中糖皮质激素诱导的骨质疏松症(GIOP)是最为常见的后果。此前研究表明,苍术内酯 I(Atractylenolide I,Atr I)具有抗炎、抗氧化和抗肿瘤特性,然而其对破骨细胞生成以及 GIOP 的具体作用仍不明确。在本研究中,体外实验结果显示,Atr I 以剂量依赖的方式抑制核因子 κB 受体活化因子配体(RANKL)刺激的破骨细胞分化,破坏成熟 ...
On March 3, 2025, the FDA approved Celltrion’s denosumab biosimilars, STOBOCLO® (denosumab-bmwo; 60 mg/mL injection) and OSENVELT® (denosumab-bmwo; ...
近年来,AKK及其巴氏杀菌形式pasteurized AKK(pAKK)因在缓解代谢疾病、炎症的潜在作用而备受关注。但是,AKK的作用并非全然有益。已有研究发现,AKK与某些自身免疫性疾病和神经系统疾病存在关联。
US FDA approves Celltrion’s Stoboclo and Osenvelt biosimilars referencing Prolia and Xgeva: Jersey City, New Jersey Wednesday, March 5, 2025, 18:00 Hrs [IST] Celltrion, a leadin ...
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The approvals for Celltrion's denosumab-bmwo (Stoboclo and Osenvelt) mark the third FDA green light for a biosimilar to treat ...
STOBOCLO ® (denosumab-bmwo) and OSENVELT ® (denosumab-bmwo) are approved by FDA for all indications of reference products ...
全人源抗PD-1单克隆抗体在实体瘤中的安全性和有效性研究。 新型RANKL抑制剂(IgG4亚型)治疗骨转移患者的疗效与安全性研究。 课题资助分类 该项目共支持约18项科研课题: 面上课题:支持4-6项,每项约12-15万元人民币,适用于单中心或中等规模多中心临床研究 ...
Denosumab is a human monoclonal antibody designed to bind to the RANKL protein, an activator of osteoclasts (cells involved in breaking down bone tissue). By binding to and inhibiting RANKL, denosumab ...
OSPOMYV™ and XBRYK™ approved by the U.S. Food and Drug Administration (FDA) for all indications referencing Prolia and Xgeva, respectively Samsung Bioepis’ first endocrinology biosimilar to be ...