FDA approves AstraZeneca's Wainua as a treatment for ATTRv-PN

22 December 2023
astrazeneca_big-1

The US Food and Drug Administration has approved AstraZeneca (LSE: AZN) and Ionis Pharmaceuticals’ (Nasdaq: IONS) Wainua (eplontersen) for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults, commonly referred to as hATTR-PN or ATTRv-PN.

AstraZeneca noted that Wainua is the only approved medicine for the treatment of ATTRv-PN that can be self-administered via an auto-injector. The UK pharma major licensed eplontersen from Ionis in December 2021, in a deal worth a potential $3.6 billion.

According to analytics firm GlobalData, the  ATTR therapy sector is forecast to reach a value of $14.1 billion across the seven major markets by 2029.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK

Today's issue

Company Spotlight





More Features in Pharmaceutical