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CompletedNCT06883656RIUpdated Mar 19, 2025

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

A Phase 1 interventional study of SAL067 in Type 2 Diabetes Mellitus (T2DM) and Renal Insuficiency, sponsored by Shenzhen Salubris Pharmaceuticals Co., Ltd.. Completed at 1 site in China. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-19.

Sponsored by Shenzhen Salubris Pharmaceuticals Co., Ltd. · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 11 months after the study started (first participant enrolled Mar 2022, registered Mar 2025).
Phase
Phase 1
Study type
Interventional
Enrollment
18
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Type 2 Diabetes Mellitus (T2DM)
  • Renal Insuficiency
03

In context

Renal Insufficiency

1,995 studies on the registry are indexed under Renal Insufficiency; 173 are open to participants now.

This study's enrollment of 18 is below the median of 43 across 1,504 interventional studies indexed under Renal Insufficiency.

Browse Renal Insufficiency studies →

Lead sponsor

Shenzhen Salubris Pharmaceuticals Co., Ltd. is the lead sponsor of 39 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  1. Age 18 to 75 (including 18 and 75 years old), both male and female;
  2. Weight: male ≥ 50 kg, female ≥ 45 kg; BMI in the range of 18 to 30 kg/m2 (including 18 and 30 kg/m2);
  3. During screening, the glomerular filtration rate (GFR) met the staging criteria of renal insufficiency or normal renal function in the corresponding group;
  4. 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.
  5. 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;
  6. 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;
  7. 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

Exclusion Criteria:

  1. People who are known to be allergic to DPP-4 inhibitors or drug excipients in this study;
  2. Previous medication history:

    1. Use of DPP-4 enzyme inhibitors or similar within 2 weeks prior to screening;
    2. Inhibitors or inducers of the CYP 2D6 enzyme used within 30 days prior to screening or required during the trial;
  3. Vaccination within 4 weeks prior to screening;
  4. 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;
  5. Hepatitis B surface antigen, hepatitis C antibody, treponema pallidum antibody, HIV antigen antibody composite test any item is positive。
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
18 participants (actual)

Study arms

  • Active comparator
    healthy subject

    Matched healthy subjects

    Drug: SAL067

  • Experimental
    Mild renal insufficiency

    Mild renal insufficiency was GFR by 60 to 89 mL/min.

    Drug: SAL067

  • Experimental
    Moderate renal insufficiency

    Moderate renal insufficiency was GFR by 30 to 59 mL/min.

    Drug: SAL067

Interventions

  • DrugSAL067

    Fasting oral test drug 12mg

06

What researchers measure

Primary outcomes

  1. Pharmacokinetic characteristics

    Peak blood concentration (Cmax)

    Time frame: 8 day

  2. Pharmacokinetic characteristics

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

    Time frame: 8 day

  3. Pharmacokinetic characteristics

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

    Time frame: 8 day

07

Study locations

1 site
  • West China Hospital of Sichuan University
    Chengdu, 61000, China
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 19, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06883656
Lead sponsor
Shenzhen Salubris Pharmaceuticals Co., Ltd.
Responsible party
Sponsor
First posted
Mar 19, 2025
Start date
Mar 15, 2022
Primary completion
Nov 1, 2022
Completion
Nov 1, 2022
Last update
Mar 19, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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