New US nod helps Takeda extend leadership in rare nerve disease

30 January 2024
takeda_hq_large

Following on from its  recent approval of Hyqvia (immune globulin) in Europe, Japanese pharma major Takeda (TYO: 4502) has picked up a US approval for another CIDP product.

Like Hyqvia, Gammagard Liquid (immune globulin) is approved to treat chronic inflammatory demyelinating polyneuropathy (CIDP), but the product is an intravenous treatment which is used as both an induction therapy and for maintenance.

Hyqvia is a novel subcutaneous product, also approved in the USA, which is used for maintenance only.

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