About Tegsedi
For your hATTR patients with stage 1 or 2 polyneuropathy, what matters is now

About Tegsedi

About Tegsedi

For your hATTR patients with stage 1 or 2 polyneuropathy, what matters is now

For your hATTR patients with stage 1 or 2 polyneuropathy, what matters is now


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Mode of Action

Mode of Action

Tegsedi targets TTR production in hATTR1,2

Efficacy

Efficacy

Tegsedi significantly delay disease progression vs placebo1

Safety

Safety

Up to 6 years of experience in clinical trials and over 220 patients years3

Administration

Administration

Tegsedi is administered as a convenient weekly subcutaneous injection1,2

About hATTR

About hATTR

Hereditary transthyretin amyloidosis is a rapidly progressive and life-shortening disease

Tegsedi CONNECT

Tegsedi CONNECT

Empowering independence for people living with hATTR

References

mRNA, messenger ribonucleic acid; TTR, transthyretin.
OLE, open-label extension; TTR, transthyretin

  1. Tegsedi Summary of Product Characteristics. April 2021.
  2. Benson MD et al. Inotersen Treatment for Patients with Hereditary Transthyretin Amyloidosis. N Engl J Med. 2018;379(1):22–31.
  3. Coelho T et al. Efficacy and safety with >3 years of inotersen treatment for the polyneuropathy of hereditary transthyretin amyloidosis. OPR15, 7th Congress of the European Academy of Neurology 2021, 19-22 June 20.