Elevar Therapeutics, Inc., Salt Lake City, UT, USA.
DUCK FLATS Pharma, Flemington, NJ, USA.
Fundam Clin Pharmacol. 2022 Feb;36(1):171-181. doi: 10.1111/fcp.12707. Epub 2021 Jul 6.
Rivoceranib is a selective inhibitor of VEGFR-2 being developed for the treatment of solid tumor. The objective of the study was to evaluate the effect of food on bioavailability as well as single- and multiple-dose pharmacokinetics (PKs) of 81 and 201 mg doses of rivoceranib. The study was conducted as a two-part study. In Part 1 (single ascending dose (SAD), open-label, crossover study design), 2 oral doses of rivoceranib (81 mg or 201 mg) were given to all healthy subjects with a minimum 3-day washout period between dosing. Part 2 was a multiple ascending dose (MAD), open-label, crossover design where subjects were divided based on 81 and 201 mg doses. Both doses were administered with and without food in a crossover manner for the SAD and MAD parts. 24 healthy subjects completed Part 1 and 20 subjects completed Part 2. For the 81 mg dose in the SAD and MAD parts of the study, their food effect was not observed. For the 201 mg dose in both parts, food appeared to increase bioavailability by 20%-30% in Part 1, and 30%-40% in Part 2. Median t value was delayed when rivoceranib was administered with food at each dose level in both parts of the study. Dose proportionality was confirmed only for the AUC value from Part 1-fasted cohort but inconclusive for C and AUC parameters under other dosing regimens. In conclusion, rivoceranib when taken with food delays t appears to increase bioavailability at 201 mg dose.
里沃卡尼伯是一种选择性血管内皮生长因子受体-2 抑制剂,用于治疗实体瘤。本研究的目的是评估食物对 81mg 和 201mg 剂量里沃卡尼伯生物利用度以及单剂量和多剂量药代动力学(PK)的影响。该研究分为两部分进行。在第一部分(单次递增剂量(SAD)、开放标签、交叉设计研究)中,所有健康受试者接受了 2 种口服剂量的里沃卡尼伯(81mg 或 201mg),两次给药之间至少有 3 天的洗脱期。第二部分是一个多递增剂量(MAD)、开放标签、交叉设计,根据 81mg 和 201mg 剂量将受试者进行分组。SAD 和 MAD 部分均以交叉方式给予两种剂量,有或无食物。24 名健康受试者完成了第一部分,20 名受试者完成了第二部分。在研究的 SAD 和 MAD 部分,81mg 剂量没有观察到食物的影响。对于 201mg 剂量,在两部分中,食物似乎使生物利用度增加了 20%-30%,在第二部分中增加了 30%-40%。在研究的两部分中,当里沃卡尼伯与食物一起给药时,每个剂量水平的中位 t 值均延迟。仅在第一部分-禁食队列的 AUC 值中证实了剂量比例性,但在其他给药方案下的 C 和 AUC 参数下结论不确定。总之,里沃卡尼伯与食物一起服用时,t 值延迟,似乎增加了 201mg 剂量的生物利用度。