Department of Research, Viventia Biotechnologies, Inc., Winnipeg, Manitoba, Canada.
Cancer Biother Radiopharm. 2012 Nov;27(9):582-92. doi: 10.1089/cbr.2012.1200.271. Epub 2012 Aug 2.
VB6-845 is a recombinant immunotoxin comprised of deBouganin (a de-immunized plant toxin) genetically linked to an epithelial cell adhesion molecule (EpCAM)-targeting humanized Fab fragment (4D5MOCB). EpCAM is highly expressed on a wide range of epithelial tumors but has limited expression on most normal epithelia and therefore represents an excellent target for immunotherapy. A comprehensive preclinical evaluation was performed to determine the safety and suitability of VB6-845 as a systemically administered drug for the treatment of solid tumors. Efficacy studies in mice demonstrated that VB6-845 specifically and potently targeted EpCAM-positive tumors. In a dose-ranging study in Sprague-Dawley rats, single doses of VB6-845 were well-tolerated resulting in a no-observable adverse effect level (NOAEL) of 100 mg/kg whereas repeated doses of VB6-845 resulted in vascular leak-associated symptoms particularly at higher dose levels. However, much higher doses in Cynomolgus monkeys were well-tolerated when given as a 3-hour infusion mimicking the intended route of administration in the clinic. In addition, VB6-845 proved to be minimally immunogenic in monkeys. The toxicological data obtained in Cynomolgus monkeys indicated an excellent safety profile with a NOAEL value of 30 mg/kg (equivalent to a 10 mg/kg dose in humans). These results are supportive of an exploratory Phase I trial.
VB6-845 是一种重组免疫毒素,由去免疫植物毒素 deBouganin 与靶向上皮细胞黏附分子 (EpCAM) 的人源化 Fab 片段 (4D5MOCB) 通过基因连接而成。EpCAM 在广泛的上皮肿瘤中高度表达,但在上皮组织中表达有限,因此是免疫治疗的理想靶点。我们进行了全面的临床前评估,以确定 VB6-845 作为治疗实体瘤的全身性药物的安全性和适用性。在小鼠的疗效研究中,VB6-845 特异性地靶向 EpCAM 阳性肿瘤,并具有强大的疗效。在 Sprague-Dawley 大鼠的剂量范围研究中,VB6-845 的单剂量耐受良好,导致 100mg/kg 的无观察不良效应水平 (NOAEL),而 VB6-845 的重复剂量导致与血管渗漏相关的症状,特别是在较高剂量水平。然而,当在恒河猴中以模拟临床给药途径的 3 小时输注给予更高剂量时,恒河猴耐受良好。此外,VB6-845 在猴子中表现出最小的免疫原性。在恒河猴中获得的毒理学数据表明具有极好的安全性,NOAEL 值为 30mg/kg(相当于人类 10mg/kg 剂量)。这些结果支持探索性 I 期试验。