A phase 1, randomized, double-blind, placebo-controlled trial investigating the pharmacokinetics, pharmacodynamics, safety and tolerability of oral semaglutide in healthy Chinese subjects

被引:3
作者
Xie, Panpan [1 ,2 ]
Abildlund, Morten T. [3 ]
Baekdal, Tine A. [3 ]
He, Xuemei [1 ,2 ]
Lyauk, Yassine K. [3 ,6 ]
Patted, Usha Rani H. [4 ]
Ning, Zu [5 ]
Shi, Aixin [1 ,2 ]
机构
[1] Beijing Hosp, Clin Trial Ctr, Natl Ctr Gerontol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Inst Geriatr Med, Beijing, Peoples R China
[3] Novo Nord AS, Soborg, Denmark
[4] Novo Nordisk Serv Ctr India Private Ltd, Bangalore, India
[5] Novo Nordisk China Pharmaceut Co Ltd, Beijing, Peoples R China
[6] Simulat Plus, Lancaster, CA USA
关键词
glucagon-like peptide-1 analogue; pharmacodynamics; pharmacokinetics; population study; randomized trial; semaglutide; ONCE-WEEKLY SEMAGLUTIDE; OPEN-LABEL; JAPANESE PATIENTS; ADD-ON; EFFICACY; 3A; DULAGLUTIDE; METFORMIN; 56-WEEK;
D O I
10.1111/dom.15624
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimThe trial (NCT04016974) investigated the pharmacokinetics, pharmacodynamics, safety and tolerability of oral semaglutide, the first orally administered glucagon-like peptide-1 analogue for type 2 diabetes, in healthy Chinese subjects.Materials and MethodsThis single-centre, multiple-dose, placebo-controlled trial randomized 32 healthy Chinese adults to once-daily oral semaglutide (3 mg escalating to 14 mg) or placebo for 12 weeks. Blood samples were collected regularly during treatment and follow-up. The primary endpoint was the area under the semaglutide concentration-time curve over a dosing interval (0-24 h) at steady state (AUC0-24h,sema,SS). Secondary pharmacokinetic endpoints included the maximum observed semaglutide plasma concentration at steady state (Cmax,sema,SS). Supportive secondary pharmacodynamics endpoints included changes in body weight and fasting plasma glucose.ResultsTreatment with all oral semaglutide doses showed dose-dependent increases in semaglutide exposure in healthy Chinese subjects at steady state, determined by AUC0-24h,sema,SS (233, 552 and 1288 h<middle dot>nmol/L for 3, 7 and 14 mg of oral semaglutide, respectively) and Cmax,sema,SS. Oral semaglutide treatment was associated with significant reductions in body weight (p = .0001) and fasting plasma glucose (p = .0011) versus placebo at the end of treatment. The safety and tolerability of oral semaglutide were consistent with the known profile of glucagon-like peptide-1 receptor agonists, with no severe or blood-glucose-confirmed symptomatic hypoglycaemic events, serious adverse events or deaths. The most frequent adverse events were gastrointestinal disorders.ConclusionsAt steady state, oral semaglutide exposure was dose dependent and close to dose proportionality in healthy Chinese subjects. This is consistent with previous clinical pharmacology results for oral semaglutide.
引用
收藏
页码:3068 / 3077
页数:10
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