Eli Lilly will withdraw its sepsis medication Xigris following results from a recent study that showed no benefit in taking the drug.

The PROWESS-SHOCK study, which enrolled 1,696 patients, showed the drug did not meet the primary endpoint of a statistically-significant reduction in 28-day all-cause mortality in patients suffering from septic shock.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

Lilly undertook the trial in order to gain continued market authorisation for Europe following its 2002 approval but the drug, which was originally approved for use in the US in November 2001, will now be withdrawn.

Once touted as a potential blockbuster, Xigris achieved sales of $104m last year.

Lilly now expects to incur a charge of between $75-95m due to the withdrawl.

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

Pharmaceutical Technology Excellence Awards - The Benefits of Entering

Gain the recognition you deserve! The Pharmaceutical Technology Excellence Awards celebrate innovation, leadership, and impact. By entering, you showcase your achievements, elevate your industry profile, and position yourself among top leaders driving pharmaceutical advancements. Don’t miss your chance to stand out—submit your entry today!

Nominate Now