Bright hopes fade for orphan drug, but Aeglea stays positive

7 December 2021
aeglea_big

Despite hitting its primary endpoint, results from the Phase III PEACE trial were not strong enough for investors, denting stock in Texan biotech Aeglea BioTherapeutics (Nasdaq: AGLE) on Monday.

Aeglea is developing pegzilarginase for the treatment of people with Arginase 1 deficiency (ARG1-D), a rare, debilitating and progressive disease.

Data from PEACE showed a statistically-significant reduction in plasma arginine from baseline after 24 weeks, as well as a positive trend in gross motor function.

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