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EMA Product

Tegsedi

Product approved by European Medicines Agency (EU)

Basic Information

Tegsedi

Regulatory Information

EMEA/H/C/004782

Authorised

July 6, 2018

May 30, 2018

15

January 17, 2024

Company Information

Ireland

St. James House 72 Adelaide Road Dublin 2 D02 Y017

AKCEA THERAPEUTICS IRELAND LIMITED

Drug Classification

Orphan MedicineAccelerated Assessment

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of stage 1 or Stage 2 polyneuropathy in adult patients with hereditary transthyretin amyloidosis (hATTR).

Overview Summary

Tegsedi is a medicine used to treat nerve damage caused by hereditary transthyretin amyloidosis (hATTR), a disease in which proteins called amyloids build up in tissues around the body including around the nerves. Tegsedi is used in adult patients in the first two stages of the nerve damage (stage 1, when the patient is able to walk unaided, and stage 2, when the patient can still walk but needs help). hATTR is rare, and Tegsedi was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 26 March 2014.

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