🇪🇺 SYR-322-4833 BL in European Union

EMA authorised SYR-322-4833 BL on 19 September 2013

Marketing authorisation

EMA — authorised 19 September 2013

  • Application: EMEA/H/C/002178
  • Marketing authorisation holder: Takeda Pharma A/S
  • Local brand name: Incresync
  • Indication: Incresync is indicated as a second- or third-line treatment in adult patients aged 18 years and older with type-2 diabetes mellitus: as an adjunct to diet and exercise to improve glycaemic control in adult patients (particularly overweight patients) inadequately controlled on pioglitazone alone, and for whom metformin is inappropriate due to contraindications or intolerance; in combination with metformin (i.e. triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in adult patients (particularly overweight patients) inadequately controlled on their maximal
  • Status: approved

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Frequently asked questions

Is SYR-322-4833 BL approved in European Union?

Yes. EMA authorised it on 19 September 2013.

Who is the marketing authorisation holder for SYR-322-4833 BL in European Union?

Takeda Pharma A/S holds the EU marketing authorisation.