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
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.
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 →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.
Exclusion Criteria:
Previous medication history:
Matched healthy subjects
Drug: SAL067
Mild renal insufficiency was GFR by 60 to 89 mL/min.
Drug: SAL067
Moderate renal insufficiency was GFR by 30 to 59 mL/min.
Drug: SAL067
Fasting oral test drug 12mg
Pharmacokinetic characteristics
Peak blood concentration (Cmax)
Time frame: 8 day
Pharmacokinetic characteristics
Area under the curve from 0 to the last time point t (AUC0-last)
Time frame: 8 day
Pharmacokinetic characteristics
Area under the curve from 0 to infinity (AUC0-inf)
Time frame: 8 day
Plan to share: No
No publications or documents are linked to this record.
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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Shenzhen Salubris Pharmaceuticals Co., Ltd.