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EMA Product

Inaqovi

Product approved by European Medicines Agency (EU)

Basic Information

Inaqovi

Regulatory Information

EMEA/H/C/005823

Authorised

September 15, 2023

July 20, 2023

3

November 30, 2023

Company Information

Netherlands

Herikerbergweg 292 1101 CT Amsterdam

Otsuka Pharmaceutical Netherlands B.V.

Drug Classification

Additional Monitoring

Active Substances Detail

cedazuridinedecitabine

Detailed Information

Therapeutic Indication

### Therapeutic indication Inaqovi is indicated as monotherapy for the treatment of adult patients with newly diagnosed acute myeloid leukaemia (AML) who are ineligible for standard induction chemotherapy.

Overview Summary

Inaqovi is a cancer medicine used in adults to treat newly diagnosed acute myeloid leukaemia (AML), a type of cancer affecting the white blood cells. It is used in patients who are not eligible for standard induction chemotherapy (initial treatment with cancer medicines). Inaqovi contains two active substances, decitabine and cedazuridine.

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