Eli Lilly Refines Pain Pipeline, Discontinues Mid-Stage P2X7 Inhibitor

Pharmaceutical giant Eli Lilly has announced another significant shift in its pain management pipeline, discontinuing development of a mid-stage P2X7 receptor inhibitor. This move comes as part of the company's ongoing efforts to refine its analgesic portfolio and focus on more promising candidates.
LY3857210 Halted After Disappointing Results
Eli Lilly has confirmed the discontinuation of LY3857210, an orally available P2X7 receptor inhibitor, citing insufficient data to meet the company's "high internal bar for success." The drug, originally licensed from Asahi Kasei Pharma in 2021 for $20 million upfront, had completed a Phase II master protocol study covering chronic low back pain, osteoarthritis pain, and diabetic peripheral neuropathic pain.
Despite the setback in pain management, Lilly is exploring potential applications for LY3857210 in other therapeutic areas. The partnership with Asahi Kasei remains intact, according to a spokesperson for the Japanese pharmaceutical company.
Strategic Pipeline Adjustments
This is not the first mid-stage pain asset Lilly has removed from its pipeline in recent months. In August, the company discarded mazisotine, a Phase II oral SSTR4 agonist that had also completed a chronic pain master protocol study. These decisions reflect Lilly's commitment to maintaining a high standard for advancement in its pain management portfolio.
Despite these cuts, Lilly continues to invest in its pain pipeline. Notable developments include:
- The acquisition of SiteOne Therapeutics in May, potentially worth up to $1 billion, which brought the Phase I Nav1.8 blocker STC-004 into Lilly's portfolio.
- Ongoing development of an anti-epiregulin antibody in mid-stage trials.
- Positioning of the oral obesity drug orforglipron for knee osteoarthritis pain, with late-stage studies expected to complete in 2027.
Financial Performance and Future Outlook
While Lilly refines its pain management strategy, the company's financial performance continues to impress. In the third quarter, Lilly reported revenues of $17.6 billion, driven largely by its blockbuster weight-loss franchise. The combined sales of Mounjaro and Zepbound reached $10.1 billion worldwide, surpassing Merck's cancer drug Keytruda ($8.1 billion) as the top-selling pharmaceutical product globally.
As Eli Lilly navigates the challenges of drug development in the pain management sector, the company's strong financial position and diverse pipeline suggest a continued focus on innovation and strategic growth in the pharmaceutical industry.
References
- Lilly Refines Pain Pipeline Again, Scrapping Mid-Stage Program
Before being discontinued, the P2X7 receptor blocker had cleared a master protocol study in chronic pain, though Eli Lilly said that results were not sufficient for advancement of the Asahi Kasei–partnered asset.
- Eli Lilly sidelines midstage prospect in another pain pipeline pivot
Eli Lilly has halted development of a phase 2 P2X7 inhibitor for pain in the latest shakeup to a pipeline that has already seen significant pivots this year.
Explore Further
What were the specific clinical trial results that led to Eli Lilly's decision to discontinue the development of LY3857210?
What is the anticipated market size for the pain management drugs still in Eli Lilly's pipeline, such as the Nav1.8 blocker STC-004?
How does Eli Lilly's partnership with Asahi Kasei impact the development and exploration of LY3857210 for other therapeutic areas?
What distinguishes Eli Lilly's anti-epiregulin antibody in mid-stage trials from similar treatments in the pain management market?
How does Eli Lilly's financial strength, driven by weight-loss drugs, contribute to its ability to invest in pain management R&D and adjust its pipeline?