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EMA Product

Isturisa

Product approved by European Medicines Agency (EU)

Basic Information

Isturisa

Regulatory Information

EMEA/H/C/004821

Authorised

January 9, 2020

November 14, 2019

7

December 12, 2024

Company Information

France

Immeuble le Wilson 70, avenue du Général de Gaulle 92800 Puteaux

RECORDATI RARE DISEASES

Drug Classification

Orphan Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Isturisa is indicated for the treatment of endogenous Cushing’s syndrome in adults.

Overview Summary

Isturisa is a medicine used to treat adults with Cushing’s syndrome, a disease characterised by an excess production of the hormone cortisol by the adrenal glands, two glands situated above the kidneys. Cushing’s syndrome is rare, and Isturisa was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 15 October 2014. Isturisa contains the active substance osilodrostat.

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