A Phase 4 interventional study of Metformin and Dapagliflozin in Diabetes Mellitus and Hypoglycemic Episodes, sponsored by Research Clinical Centre of the Russian Railways, JSC. Status unknown at 1 site in Russia. Open to participants aged 18 Years to 74 Years. Per ClinicalTrials.gov, last updated 2016-03-25.
Sponsored by Research Clinical Centre of the Russian Railways, JSC · Phase 4 and Interventional
This study will test the hypothesis that early use of combination therapy with dapagliflozin and metformin will provide good glycemic control with low glycemic variability and without hypoglycemic episodes, and will be better tolerated than up-titration of metformin monotherapy. The study will also correlate these benefits with glycated hemoglobin.
Type 2 diabetes is a progressive, chronic metabolic disease characterized by hyperglycemia. Despite therapeutic advances, the incidence and prevalence of diabetes continue to surge. Worldwide, the number of individuals with diabetes is projected to rise from 366 million in 2011 to 552 million by 2030, which is the equivalent of approximately three new cases being diagnosed every 10 seconds. Type 2 diabetes doubles the risk of cardiovascular disease, and macrovascular complications (myocardial infarction and stroke) are a common cause of death in patients with type 2 diabetes. The U.K. Prospective Diabetes Study showed that every 1% absolute decline in mean A1C was associated with a 37% reduction in the risk of microvascular complications and a 21% reduction in the risk of any diabetes-related complication or death. Diabetes also exacts a tremendous economic burden. Meeting treatment goals is elusive for many people with diabetes. Data from the National Health and Nutrition Examination Survey from 2003 to 2006 showed that only 57.1% of adults with diagnosed diabetes achieved an A1C \< 7%, 45.5% had a blood pressure level \< 130/80 mmHg, and 46.5% had an LDL cholesterol level \< 100 mg/dl. Only 12.2% of people with diabetes reached all three goals. Treatment of Type 2 diabetes is not limited to just glycaemic control. Rather, the proper management of hyperglycaemia, weight, blood pressure, and lipids can have benefits in terms of slowing the progression of Type 2 diabetes, decreasing the risk of CV disease, and improving overall health.Current antihyperglycaemic treatments are predominantly insulin-dependent. These treatments can effectively manage HbA1c, and treatment may be influenced by the patient's comorbidities and any potential treatment-related adverse events. However, as Type 2 diabetes progresses, regimens need to be modified to compensate for declining beta-cell function and decreasing insulin sensitivity. On this basis,the EASD/ADA guidelines suggest following a treatment pathway that has well validated therapies at it's core.Of the many comorbid conditions described, excess weight is especially important, not only because of the increased disease risk, but also for the management of blood pressure and lipids. Consequently, AACE/ACE algorithms give priority to those regimens that have the added benefit of minimising hypoglycaemic events and weight gain.In addition, while antidiabetic treatments tend to focus on insulin-dependent mechanisms in organs such as the liver and pancreas, it should not be forgotten that the kidneys also have a role in maintaining glucose homeostasis There are multiple barriers to achieving optimal glycemic control. Current medications for type 2 diabetes have potential adverse effects; for example, can cause hypoglycemia and weight gain. Hypoglycaemia is a limiting factor in the glycaemic management of patients with advanced Type 2 diabetes.Most often hypoglycaemia is associated with mild to severe neurologic symptoms, and in some cases it can result in death. Additionally, the risk of cardiac ischaemia is increased in Type 2 diabetes patients with symptomatic or asymptomatic hypoglycaemia compared with patients with hyperglycaemia or stable normoglycaemia. The risk of hypoglycaemia increases with advancing age, polypharmacy, later stages of disease, and intensive antihyperglycaemic treatment with certain drugs, such as sulphonylureas. Intensive treatment (target HbA1c\<7.0%) results in a greater number of patients experiencing severe hypoglycaemic events (3-21%) compared with conventional treatment (target HbA1c ≥7.0%; 2-10%), although intensive therapy may have a greater beneficial effect in terms of a decreased risk of microvascular disease. As a result, hypoglycaemia is one of several factors, including weight gain and increases in CV disease-related and overall mortality, that may limit the microvascular benefits of intensive therapy. Thus, the search continues for novel therapeutic agents that can help patients avoid these limiting side effects while providing glycemic control.
11,089 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.
This study's planned enrollment of 100 is above the median of 80 across 8,491 interventional studies indexed under Diabetes Mellitus.
Browse Diabetes Mellitus studies →Research Clinical Centre of the Russian Railways, JSC is the lead sponsor of 2 studies on the registry; none are open to participants now.
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The subject population that will be observed in the study, must fulfil all of the following criteria:
Exclusion criteria
The presence of absolute contraindications to therapy by SGLT-2 inhibitor Dapagliflozin:
1.1. Individual idiosyncrasy of any drug component.
1.2. Type 1 diabetes.
1.3. Diabetic ketoacidosis.
1.4. Renal disease, medium to severe (eGFR \<60 ml/min /1.73m2 by MDRD formula) or end-stage renal failure.
1.5.Hereditary lactose intolerance, lactase deficiency, and glucose and galactose intolerance.
1.6. Pregnancy and breast-feeding.
1.7. Children under 18 years of age.
1.8. Patients receiving loop diuretics or with reduced volume of blood circulation, such as a result of acute diseases (e.g. gastrointestinal problems).
1.9. Elderly patients aged 75 years and older.
Metformin stable dose tablets and Dapagliflozin 10 mg tablets by mouths, once daily in morning for 3 months
Drug: Metformin · Drug: Dapagliflozin
Metformin tablets up-titration by mouths, for 3 months
Drug: Metformin · Drug: Metformin up-titration
Metformin tablets 1000 mg
Also known as: GLUCOPHAGE
Dapagliflozin 10 mg tablets
Also known as: FORXIGA, FARXIGA
Dynamics (delta from the baseline) of blood glucose variability - integral index of glycemia (LBGI-HBGI) after 3 months of therapy
Time frame: 3 months
Dynamics (delta from the baseline or % decrease of blood glucose level) of blood glucose variability (ADRR) after 3 months of therapy
Time frame: 3 months
Dynamics of MAGE after 3 months of therapy
Time frame: 3 months
Dynamic of glycaemia parameters: % of normoglycemia time after 3 months of therapy
Time frame: 3 months
Dynamic of glycaemia parameters: % of hyperglycemia time after 3 months of therapy
Time frame: 3 months
Dynamic of glycaemia parameters: % of hypoglycemia time after 3 months of therapy
Time frame: 3 months
Dynamics of HbA1c (%) from baseline after 3 months of therapy
Time frame: 3 months
Percentage of diabetes mellitus patients achieved individual target HbA1c
Time frame: 3 months
Plan to share: No
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This study is status unknown, as verified in Mar 2016. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Dapagliflozin
Research Clinical Centre of the Russian Railways, JSC