New drug data tightens Alexion's grip on market for rare blood disorder

15 March 2018
2019_biotech_test_vial_discovery_big

Fears that competition could soon hit sales of Soliris (eculizumab) will probably feel less acute at US drugmaker Alexion Pharmaceuticals (Nasdaq: ALXN) after the company presented data on a new drug that could prolong its dominance in a rare blood disorder.

Alexion is conducting a Phase III trial comparing ALXN1210, its investigational long-acting C5 complement inhibitor, to Soliris in complement inhibitor treatment-naïve patients with paroxysmal nocturnal hemoglobinuria (PNH).

"We expect the market to transition almost entirely to the longer-acting product within six to 12 months of its introduction in each market"

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 Biotechnology