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EMA Product

Cinryze

Product approved by European Medicines Agency (EU)

Basic Information

Cinryze

Regulatory Information

EMEA/H/C/001207

Authorised

June 15, 2011

March 17, 2011

24

September 26, 2024

Company Information

Austria

Industriestrasse 67 1221 Vienna

Takeda Manufacturing Austria AG

Drug Classification

Additional Monitoring

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment and pre-procedure prevention of angioedema attacks in adults, adolescents and children (2 years old and above) with hereditary angioedema (HAE). Routine prevention of angioedema attacks in adults, adolescents and children (6 years old and above) with severe and recurrent attacks of hereditary angioedema (HAE), who are intolerant to or insufficiently protected by oral prevention treatments, or patients who are inadequately managed with repeated acute treatment.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Cinryze. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Cinryze.

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