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EMA Approval

Eucreas

A10BD08

metformin and vildagliptin

vildagliptinmetformin

Diabetes Mellitus, Type 2

vildagliptinmetformin hydrochloride

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.

Authorisations (2)

EMEA/H/C/000807

Novartis Europharm Limited,Vista Building,Elm Park,Merrion Road,Dublin 4,Ireland

Authorised

November 14, 2007

EMEA/H/C/000807

Novartis Europharm Limited,Vista Building,Elm Park,Merrion Road,Dublin 4,Ireland

Authorised

November 14, 2007

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.

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