1 Blaze Bioscience, Inc, Seattle, WA, USA.
2 Northwest PK Solutions, LLC, Sultan, WA, USA.
Int J Toxicol. 2017 Mar/Apr;36(2):104-112. doi: 10.1177/1091581817697685. Epub 2017 Mar 17.
BLZ-100 is a single intravenous use, fluorescent imaging agent that labels tumor tissue to enable more complete and precise surgical resection. It is composed of a chlorotoxin peptide covalently bound to the near-infrared fluorophore indocyanine green. BLZ-100 is in clinical development for intraoperative visualization of human tumors. The nonclinical safety and pharmacokinetic (PK) profile of BLZ-100 was evaluated in mice, rats, canines, and nonhuman primates (NHP). Single bolus intravenous administration of BLZ-100 was well tolerated, and no adverse changes were observed in cardiovascular safety pharmacology, PK, and toxicology studies in rats and NHP. The single-dose no-observed-adverse-effect-levels (NOAELs) were 7 mg (28 mg/kg) in rats and 60 mg (20 mg/kg) in NHP, corresponding to peak concentration values of 89 400 and 436 000 ng/mL and area-under-the-curve exposure values of 130 000 and 1 240 000 h·ng/mL, respectively. Based on a human imaging dose of 3 mg, dose safety margins are >100 for rat and monkey. BLZ-100 produced hypersensitivity reactions in canine imaging studies (lethargy, pruritus, swollen muzzle, etc). The severity of the reactions was not dose related. In a follow-up study in dogs, plasma histamine concentrations were increased 5 to 60 minutes after BLZ-100 injection; this coincided with signs of hypersensitivity, supporting the conclusion that the reactions were histamine based. Hypersensitivity reactions were not observed in other species or in BLZ-100 human clinical studies conducted to date. The combined imaging, safety pharmacology, PK, and toxicology studies contributed to an extensive initial nonclinical profile for BLZ-100, supporting first-in-human clinical trials.
BLZ-100 是一种单次静脉使用的荧光成像剂,可标记肿瘤组织,从而实现更完整、更精准的手术切除。它由氯毒素肽与近红外荧光染料吲哚菁绿共价结合而成。BLZ-100 正处于用于人类肿瘤术中可视化的临床开发阶段。在小鼠、大鼠、犬和非人灵长类动物(NHP)中评估了 BLZ-100 的非临床安全性和药代动力学(PK)特征。BLZ-100 单次静脉推注后耐受性良好,在大鼠和 NHP 的心血管安全性药理学、PK 和毒理学研究中未观察到不良反应。大鼠和 NHP 的单次剂量无观察到不良反应水平(NOAEL)分别为 7mg(28mg/kg)和 60mg(20mg/kg),相应的峰浓度值分别为 89400ng/mL 和 436000ng/mL,曲线下面积暴露值分别为 130000h·ng/mL 和 1240000h·ng/mL。基于 3mg 的人体成像剂量,大鼠和猴的剂量安全性裕度均>100。BLZ-100 在犬的成像研究中引起了过敏反应(嗜睡、瘙痒、肿胀的口鼻等)。反应的严重程度与剂量无关。在犬的后续研究中,BLZ-100 注射后 5-60 分钟,血浆组胺浓度升高;这与过敏反应的迹象一致,支持反应基于组胺的结论。在其他物种或迄今为止进行的 BLZ-100 人体临床研究中未观察到过敏反应。综合成像、安全药理学、PK 和毒理学研究为 BLZ-100 提供了广泛的初始非临床特征,支持首次人体临床试验。