Basic Information
A10BD08
metformin and vildagliptin
Therapeutic indication
Eucreas is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:
- in patients who are inadequately controlled with metformin hydrochloride alone.
- in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets.
- in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control
Overview Summary
Eucreas is a diabetes medicine that is used together with diet and exercise to control the blood glucose (sugar) in adults with type 2 diabetes. It is used:
- in patients whose blood glucose is insufficiently controlled with metformin taken alone;
- in patients who are already taking the combination of vildagliptin and metformin as separate tablets;
- together with other diabetes medicines, including insulin, when these medicines do not provide adequate control of the blood glucose.
Eucreas contains the active substances vildagliptin and metformin hydrochloride.
Active Substances (3)
vildagliptinmetformin hydrochloride
vildagliptin
metformin hydrochloride
Documents (18)
Eucreas : EPAR - Scientific Discussion
December 2, 2007
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas : EPAR - Procedural steps taken before authorisation
December 2, 2007
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Eucreas : EPAR - Procedural steps taken before authorisation
December 2, 2007
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas-H-C-807-WS-0257 : EPAR - Assessment Report - Variation
February 19, 2013
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas-H-C-807-WS-0272 : EPAR - Assessment Report - Variation
February 19, 2013
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP post-authorisation summary of positive opinion for Eucreas (WS-1937-G)
May 21, 2021
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas : EPAR - Scientific Discussion
December 2, 2007
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Eucreas : EPAR - Medicine overview
December 2, 2007
OVERVIEW_DOCUMENT
Eucreas-H-C-807-A31-1432 : EPAR - Scientific Conclusion
January 12, 2017
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas : EPAR - All Authorised presentations
December 2, 2007
AUTHORISED_PRESENTATIONS
Eucreas : EPAR - Procedural steps taken and scientific information after authorisation (archive)
September 20, 2009
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas : EPAR - Procedural steps taken and scientific information after authorisation
February 3, 2025
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP post-authorisation summary of positive opinion for Eucreas
September 20, 2012
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas-H-C-PSUSA-00003113-201502 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation
January 7, 2016
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas-H-C-807-WS-1937-G: EPAR - Assessment Report - Variation
August 24, 2021
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas : EPAR - Risk-management-plan summary
March 29, 2023
RISK_MANAGEMENT_PLAN_SUMMARY
Eucreas-H-C-807-A31-1432 : EPAR - Assessment Report - Article 31
January 12, 2017
CHANGES_SINCE_INITIAL_AUTHORISATION
Eucreas : EPAR - Product Information
September 20, 2009
DRUG_PRODUCT_INFORMATION
Overview Q&A (7)
Question
Other information about Eucreas
Answer
Eucreas received a marketing authorisation valid throughout the EU on 14 November 2007.
Question
How is Eucreas used?
Answer
Eucreas is available as tablets (50 mg/850 mg and 50 mg/1,000 mg), and the recommended dose is one tablet twice a day (one in the morning and one in the evening). The starting tablet strength depends on the patient’s current treatment and the expected effects of Eucreas. Taking Eucreas with or just after food may reduce any stomach problems caused by metformin.
The doctor should carry out tests to check the patient’s kidney and liver function before treatment with Eucreas and at regular intervals during treatment.
The medicine can only be obtained with a prescription. For more information about using Eucreas, see the package leaflet or contact your doctor or pharmacist.
Question
How does Eucreas work?
Answer
Type 2 diabetes is a disease in which the pancreas does not make enough insulin to control the glucose level in the blood or the body is unable to use insulin effectively. Eucreas contains two active substances, each with a different mode of action.
Vildagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that works by blocking the breakdown of incretin hormones in the body. These hormones are released after a meal and stimulate the pancreas to produce insulin. By blocking the breakdown of incretin hormones in the blood, vildagliptin prolongs their action, stimulating the pancreas to produce more insulin when blood glucose levels are high. Vildagliptin does not work when the blood glucose is low. Vildagliptin also reduces the amount of glucose made by the liver by increasing insulin levels and decreasing the levels of the hormone glucagon.
Metformin works mainly by inhibiting glucose production and reducing its absorption in the gut. As a result of the action of both substances, the blood glucose is reduced, which helps to control type 2 diabetes.
Question
What benefits of Eucreas have been shown in studies?
Answer
Vildagliptin on its own is approved for use in the EU under the name Galvus, and metformin has been available in the EU since 1959. Vildagliptin can be used with metformin in type 2 diabetes patients who are not satisfactorily controlled on metformin alone.
Studies with Galvus as an add-on to metformin, metformin and a sulphonylurea, or metformin and insulin have been used to support the use of Eucreas in the same indications. The studies compared Galvus with placebo (a dummy treatment) and measured the levels of a substance in the blood called glycosylated haemoglobin (HbA1c), which gives an indication of how well the blood glucose is controlled.
Vildagliptin has been shown to be more effective than placebo at reducing HbA1c levels when it was added to metformin. Patients adding vildagliptin had falls in HbA1c levels of 0.88 percentage points after 24 weeks from a starting level of 8.38%. In contrast, patients adding placebo had smaller changes in HbA1c levels, with a rise of 0.23 percentage points from a starting level of 8.3%. In other studies, vildagliptin in combination with metformin has been shown to be more effective than placebo when used with a sulphonylurea or insulin.
The applicant also presented the results of two studies showing that the active substances in the two strengths of Eucreas were absorbed in the body in the same way as when they were taken as separate tablets.
Question
What are the risks associated with Eucreas?
Answer
The most common side effects with Eucreas (seen in more than 1 patient in 10) are nausea (feeling sick), vomiting, diarrhoea, abdominal (belly) pain and loss of appetite. For the full list of all side effects reported with Eucreas, see the package leaflet.
Eucreas must not be used in people who are hypersensitive (allergic) to vildagliptin, metformin or any of the other ingredients. Eucreas must also not be used in patients with certain kidney, liver or heart problems or those who could develop metabolic acidosis (build-up of acid in the blood). It must also not be used in patients who consume excessive amounts of alcohol or who have alcoholism, or in women who are breastfeeding. For the full list of restrictions, see the package leaflet.
Question
Why is Eucreas authorised in the EU?
Answer
Studies have shown that vildagliptin taken with metformin is effective in reducing blood glucose levels and that the combination of vildagliptin and metformin was effective as an add-on to a sulphonylurea or insulin. The combination of the two active substances vildagliptin and metformin in one tablet may help patients to stick to their treatment. The European Medicines Agency therefore decided that Eucreas’ benefits are greater than its risks and it can be authorised for use in the EU.
Question
What measures are being taken to ensure the safe and effective use of Eucreas?
Answer
Recommendations and precautions to be followed by healthcare professionals and patients for the safe and effective use of Eucreas have been included in the summary of product characteristics and the package leaflet.
As for all medicines, data on the use of Eucreas are continuously monitored. Suspected side effects reported with the medicine are carefully evaluated and any necessary action taken to protect patients.