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EMA Product

Palynziq

Product approved by European Medicines Agency (EU)

Basic Information

Palynziq

Regulatory Information

EMEA/H/C/004744

Authorised

May 3, 2019

February 28, 2019

8

July 12, 2024

Company Information

Ireland

Shanbally Ringaskiddy County Cork P43 R298

Biomarin International Limited

Drug Classification

Orphan Medicine

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Palynziq is indicated for the treatment of patients with phenylketonuria (PKU) aged 16 years and older who have inadequate blood phenylalanine control (blood phenylalanine levels greater than 600 micromol/l) despite prior management with available treatment options.

Overview Summary

Palynziq is a medicine that is used to treat phenylketonuria (PKU) in adults and adolescents from 16 years of age. Patients with this genetic disease cannot process the amino acid phenylalanine from dietary protein, and as a result the amino acid builds up in the blood to abnormally high levels, causing problems in the nervous system. Palynziq is used in patients whose blood levels of phenylalanine have not been adequately controlled with other treatments. Palynziq was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 28 January 2010. Further information on the orphan designation can be found [EU/3/09/708](/en/medicines/human/orphan-designations/eu-3-09-708). Palynziq contains the active substance pegvaliase.

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