| Name | BT7480 |
|---|
| Description | BT7480 (BCY11863) is one of the Bicycle tumor-targeted immune cell agonists (Bicycle TICAs). BT7480 is an angonist of CD137 (4-1BB). BT7480 consists of a poly(ethylene glycol) (PEG)-based linker, and a synthetic Bicycle peptide targeting CD137 conjugated to Bicycles targeting Nectin-4. Nectin-4 is a cell adhesion molecule, overexpressing in multiple tumor cells. BT7480 elicits significant CD137 agonism and potent antitumor activity in syngeneic mouse models[1][2]. |
|---|---|
| Related Catalog | |
| Target |
CD137 (4-1BB)[1] |
| In Vitro | BT7480 导致原代人免疫细胞中促炎细胞因子 IFNγ 和 IL-2 的分泌呈剂量依赖性增加 (EC50=0.22 nM 和 0.36 nM),而 HT1376 肿瘤细胞与来自健康供体的人外周血单核细胞 (PBMC) 共培养并用抗 CD3 处理以刺激 CD137 在免疫细胞上的表达[1]。 |
| In Vivo | BT7480(5 mg/kg;腹腔注射;每天一次,持续 10 天)在 CT26-Nectin-4/huCD137 小鼠模型中表现出抗肿瘤活性[1]。 BT7480(2 mg/kg;静脉注射;单剂量)的 CL 为 8.5 mL/min/kg,终末半衰期为 3.6 小时[1]。 BT7480(1、5、10 和 30 mg/kg;腹腔注射;单剂量)导致 CD-1 小鼠的暴露量 (AUCinf) 剂量依赖性增加[1] 。 BT7480(1 和 10 mg/kg;腹腔注射;每天 3 次,持续 40 天)在小鼠 MC38-Nectin-4 肿瘤模型中导致肿瘤消退[1]。 在食蟹猴 MC38 同基因模型中的药代动力学分析[1] Route Dose (mg/kg) CLlast (mL/min/kg) Vdss (L/kg) t1/2 (h) i.v. 1 3.3 0.62 5.3 Animal Model: Mice bearing subcutaneous MC38-Nectin-4 tumors[1] Dosage: 1 mg/kg and 10 mg/kg Administration: IP; 3 times per days for 40 days Result: Led efficacious tumor growth reduction and complete responses (CRs) induction, with the rate of CRs ranging from 4/6 (1 mg/kg) to 6/6 (10 mg/kg) by day 40. |
| References |
| Molecular Formula | C331H467N73O89S10 |
|---|---|
| Molecular Weight | 7213.34 |