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Completed

NCT Number: NCT06883656

The Pharmacokinetics Study of Fotagliptin in Patients with Different Degrees of Renal Insufficiency

The trial was designed in a single dose, open, non-randomized, multi-dose parallel control group. The study of patients were mild and moderate renal insufficiency, and matched healthy subjects.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

West China Hospital of Sichuan University

Chengdu, China, 61000

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 to 75 (including 18 and 75 years old), both male and female;
  • Weight: male ≥ 50 kg, female ≥ 45 kg; BMI in the range of 18 to 30 kg/m2 (including 18 and 30 kg/m2);
  • During screening, the glomerular filtration rate (GFR) met the staging criteria of renal insufficiency or normal renal function in the corresponding group;
  • The subjects can communicate well with the researchers, fully understand the purpose and requirements of the trial, voluntarily participate in the clinical trial and sign a written informed consent.
  • During screening, the investigators judged that the kidney disease of the subjects was stable from 4 weeks before screening to the end of the study, and GFR did not change significantly;
  • Patients who had not taken or were on stable medication for renal insufficiency and/or other comorbiditions during the 4 weeks prior to screening and agreed to continue treatment during the study period;
  • Patients with diabetes who have not used hypoglycemic drugs in the 4 weeks prior to screening, or who are receiving stable antidiabetic therapy (including lifestyle interventions, use of stable doses of drugs, except for prohibited drugs described in the trial protocol) and agree to continue treatment during the study period.

Exclusion criteria

  • People who are known to be allergic to DPP-4 inhibitors or drug excipients in this study;
  • Previous medication history:
  • Use of DPP-4 enzyme inhibitors or similar within 2 weeks prior to screening;
  • Inhibitors or inducers of the CYP 2D6 enzyme used within 30 days prior to screening or required during the trial;
  • Vaccination within 4 weeks prior to screening;
  • Pregnant or lactating women; The subject and his or her spouse or partner have plans to become pregnant, or plan to donate sperm or eggs, or do not agree to an acceptable and effective method of contraception within 3 months of dosing;
  • Hepatitis B surface antigen, hepatitis C antibody, treponema pallidum antibody, HIV antigen antibody composite test any item is positive。

Treatment and study plan

SAL067

Drug

Fasting oral test drug 12mg

Primary outcomes

  1. Pharmacokinetic characteristics

    Time frame: 8 day

    Peak blood concentration (Cmax)

  2. Pharmacokinetic characteristics

    Time frame: 8 day

    Area under the curve from 0 to the last time point t (AUC0-last)

  3. Pharmacokinetic characteristics

    Time frame: 8 day

    Area under the curve from 0 to infinity (AUC0-inf)

Sponsors and collaborators

Lead sponsor

Shenzhen Salubris Pharmaceuticals Co., Ltd.

Industry

Registry information

Official study title

The Pharmacokinetics Study of Fotagliptin in Patients with Different Degrees of Renal Insufficiency and Matched Healthy Volunteers with Normal Renal Function

Acronym: RI

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Mar 19, 2025
Registry last updated
Mar 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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