Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    In: British Journal of Clinical Pharmacology, Wiley, Vol. 88, No. 6 ( 2022-06), p. 2946-2958
    Abstract: This study investigated the pharmacokinetics and pharmacodynamics properties, safety and tolerability of cetagliptin. Methods Forty‐eight healthy subjects were enrolled in this study. Three cohorts were investigated in sequential order: 50, 100 and 200 mg cetagliptin. Positive control (sitagliptin 100 mg) was designed as open label. Blood samples were collected and analysed for pharmacokinetic and pharmacodynamic properties. Safety and tolerability were assessed throughout the study. Results Following multiple oral doses, cetagliptin was rapidly absorbed and reached peak plasma concentrations after approximately 1.0–1.5 hours. Plasma cetagliptin concentrations increased at a rate greater than dose. Accumulation of cetagliptin was modest, and steady state was generally achieved at day 5. Doses ≥50 mg of cetagliptin administered once daily will result in sustained dipeptidyl peptidase‐4 (DPP‐4) inhibition (≥80%). The plasma concentration giving 50% of maximum drug effect of DPP‐4 inhibition for cetagliptin (5.29 ng/mL) was lower than that of sitagliptin (7.03 ng/mL). Active glucagon‐like‐1 peptide (GLP‐1) concentrations were significantly increased in the cetagliptin groups by 2.3‐ to 3.1‐fold at day 1 and 3.1‐ to 3.6‐fold at steady state compared with that of placebo, and active GLP‐1 concentrations were increased with increasing dose. Compared with sitagliptin, doses ≥100 mg once daily of cetagliptin produced postprandial increases in active GLP‐1 level and induced to long‐lasting glucose‐lowering efficacy. Cetagliptin was well tolerated across all doses studied. Conclusion Cetagliptin demonstrates the great potential for treatment with type 2 diabetes patients based on the inhibition of DPP‐4, the increase in GLP‐1 and insulin, the decrease in glucose, and might be more effective in DPP‐4 inhibition than sitagliptin.
    Type of Medium: Online Resource
    ISSN: 0306-5251 , 1365-2125
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 1498142-7
    SSG: 15,3
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. Further information can be found on the KOBV privacy pages