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EMA Product

Pyrukynd

Product approved by European Medicines Agency (EU)

Basic Information

Pyrukynd

Regulatory Information

EMEA/H/C/005540

Authorised

November 9, 2022

September 15, 2022

December 5, 2022

Company Information

Agios Netherlands B.V.,Zuidplein 36,1077XV Amsterdam,Netherlands

Netherlands

Zuidplein 36 1077XV Amsterdam

agios netherlands b.v.

Drug Classification

Orphan MedicineAdditional Monitoring

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Pyrukynd is indicated for the treatment of pyruvate kinase deficiency (PK deficiency) in adult patients (see section 4.4).

Overview Summary

Pyrukynd is a medicine used to treat adults with pyruvate kinase deficiency (PKD), an inherited disease that causes red blood cells to break down faster than normal. PKD is rare, and Pyrukynd was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 22 April 2020. Further information on the orphan designation can be found here: [https://www.ema.europa.eu/en/medicines/human/orphan-designations/eu-3-20-2270](/en/medicines/human/orphan-designations/eu-3-20-2270). Pyrukynd contains the active substance mitapivat.

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