More bad news for selonsertib, but Gilead undeterred in NASH

26 April 2019
gilead-big

Two months after announcing a  Phase III flop for selonsertib, one of its key non-alcoholic steatohepatitis (NASH) candidates, US biotech Gilead Sciences (Nasdaq: GILD) says the drug has failed another pivotal test.

Top-line data show the STELLAR-3 study did not meet its primary endpoint, with just 9.3% of people treated with selonsertib at the higher dose, and 12.1% at the lower dose, achieving the required improvement. 13.2% of people in the placebo group met that threshold.

The firm has invested significantly in building a pipeline of NASH drugs, hoping to gain a share of what analysts expect to become a multi-billion dollar market in future years.

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