[Translation] A single-center, open-label, randomized, single-dose, two-period, two-sequence, crossover bioequivalence study evaluating the bioequivalence of the test formulation, upadacitinib extended-release tablets (15 mg), compared with the reference formulation, upadacitinib extended-release tablets (Refox®, 15 mg), in healthy adult participants under fasting and fed conditions.
主要目的:研究空腹和餐后状态下单次口服受试制剂乌帕替尼缓释片(规格:15 mg,生产厂家:南通联亚药业股份有限公司)与参比制剂乌帕替尼缓释片(瑞福®,规格:15 mg,生产厂家:AbbVie Ireland NL B.V.)在健康成年参与者体内的药代动力学,评价空腹和餐后状态下口服两种制剂的生物等效性。次要目的:评估受试制剂乌帕替尼缓释片(规格:15 mg)与参比制剂乌帕替尼缓释片(瑞福®,规格:15 mg)在健康成年参与者的安全性。
[Translation] The primary objective was to investigate the pharmacokinetics of the test formulation, upadacitinib extended-release tablets (15 mg, manufactured by Nantong Lianya Pharmaceutical Co., Ltd.), compared with the reference formulation, upadacitinib extended-release tablets (Rufu®, 15 mg, manufactured by AbbVie Ireland NL B.V.), in healthy adult participants after a single oral dose in the fasting and fed states, and to evaluate the bioequivalence of the two formulations in the fasting and fed states. The secondary objective was to evaluate the safety of the test formulation, upadacitinib extended-release tablets (15 mg), compared with the reference formulation, upadacitinib extended-release tablets (Rufu®, 15 mg), in healthy adult participants.