CLINICAL TRIALS PROFILE FOR METFORMIN HYDROCHLORIDE; SITAGLIPTIN PHOSPHATE
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All Clinical Trials for metformin hydrochloride; sitagliptin phosphate
| Trial ID | Title | Status | Sponsor | Phase | Start Date | Summary |
|---|---|---|---|---|---|---|
| NCT00466518 ↗ | Sitagliptin Treatment in Patients With Type 2 DM After Kidney Transplant | Completed | University of Nebraska | N/A | 2007-04-01 | This study is designed to look at the effect sitagliptin has on tacrolimus and sirolimus drug levels in kidney transplant patients. It is also designed to look at the side effects experienced in the transplant population. |
| NCT00466518 ↗ | Sitagliptin Treatment in Patients With Type 2 DM After Kidney Transplant | Completed | University of Oklahoma | N/A | 2007-04-01 | This study is designed to look at the effect sitagliptin has on tacrolimus and sirolimus drug levels in kidney transplant patients. It is also designed to look at the side effects experienced in the transplant population. |
| NCT01357148 ↗ | A Post Marketing Safety Study of Sitagliptin Phosphate/Metformin Hydrochloride (JANUMET®) (MK-0431A-235) | Terminated | Merck Sharp & Dohme Corp. | 2009-03-01 | The primary objective of this study is to obtain safety information on the use of sitagliptin phosphate/metformin hydrochloride (HCl) (JANUMET®) from endocrinologists, diabetologists, internists, and general practitioners. | |
| NCT03180281 ↗ | Therapies on Newly Diagnosed Type 2 Diabetes Patients With High Glucose Toxicity Which Protect Islet β Cell | Unknown status | First Affiliated Hospital Xi'an Jiaotong University | N/A | 2017-07-01 | Prevalence of diabetes is increasing rapidly both in China and all over the world.Hyperglycemia is an important risk factor and major hazard to cardiovascular and cerebrovascular diseases and even dangerous to human health."High glucose toxicity "cause pancreatic β cell non-physiologic and irreversible damage.It is an important cause of β cell dysfunction.High glucose toxicity further suppresses insulin secretion of β cell, further even β-cell function failure.It is urgent to explore more effective and safety treatments which can also protect islet cells function.How to release high glucose toxicity , reverse the toxic effects of hyperglycemia on islet β cells as early as possible, and to maximize recover and protect the pancreatic β cell function is the keypoints of this study.Our aim is to explore the non-inferiority of new antidiabetic drugs DPP4 inhibitors on releasing glucose toxicity and protecting islet β cell function compared with traditional treatments on newly diagnosed type 2 diabetes,compare efficacy and safety of different oral antidiabetic drugs and insulin on newly diagnosed type 2 diabetes patients with high glucose toxicity and compare differences of different oral antidiabetic drugs and insulin on protecting pancreatic β-cell function. |
| >Trial ID | >Title | >Status | >Sponsor | >Phase | >Start Date | >Summary |
Clinical Trial Conditions for metformin hydrochloride; sitagliptin phosphate
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Clinical Trial Progress for metformin hydrochloride; sitagliptin phosphate
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Clinical Trial Sponsors for metformin hydrochloride; sitagliptin phosphate
Sponsor Name
| Sponsor Name for metformin hydrochloride; sitagliptin phosphate | |
| Sponsor | Trials |
| First Affiliated Hospital Xi'an Jiaotong University | 1 |
| The Affiliated Hospital of Qingdao University | 1 |
| University of Nebraska | 1 |
| [disabled in preview] | 1 |
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