West China Hospital of Sichuan University
Chengdu, China, 61000
NCT Number: NCT06883656
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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Notify Me18 year–75 year
All sexes
Interventional
Phase 1
Chengdu, China, 61000
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Fasting oral test drug 12mg
Time frame: 8 day
Peak blood concentration (Cmax)
Time frame: 8 day
Area under the curve from 0 to the last time point t (AUC0-last)
Time frame: 8 day
Area under the curve from 0 to infinity (AUC0-inf)
Shenzhen Salubris Pharmaceuticals Co., Ltd.
Industry
The Pharmacokinetics Study of Fotagliptin in Patients with Different Degrees of Renal Insufficiency and Matched Healthy Volunteers with Normal Renal Function
Acronym: RI
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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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