Eli Lilly and Company announced its acquisition of Vere Therapeutics has successfully completed, following the previous day’s announcement of the expiration of the Vere tender offer.
Key Takeaways
- Lilly officially acquires Vere Therapeutics advancing developments in one-time treatment options.
- The acquisition allows for expansion in innovations for gene editing and cardiovascular medications.
- Lilly will continue to develop and expand Vere’s pipeline of medications with a focus on Vere-102.
Ruth Gimeno, Lilly group vice president, diabetes and metabolic research and development, spoke on the impact of the acquisition, saying, "This acquisition unlocks the opportunity to potentially transform the treatment paradigm for millions of patients worldwide by delivering lifelong cardiovascular risk reduction with a one-and-done treatment. We are excited to welcome Verve colleagues to Lilly and work together to develop innovative genetic medicines for cardiometabolic disease."1
The future of one-time treatments
Eli Lilly and Company officially acquired Vere Therapeutics. Originally announced back in June of 2025, both Lilly and Vere came to a definitive agreement on Lilly’s complete acquisition of Vere. Eli Lilly chose to acquire Vere due to its developing pipeline of gene editing medicines designed to address drivers of atherosclerotic cardiovascular disease (ASCVD) through one-time treatment options.
Vere’s pipeline includes its lead program Vere-102, a potential first-in-class vivo gene editing medicine that targets Pcsk9, a gene linked to cholesterol levels and cardiovascular health. This treatment option is deemed applicable to those who have heterozygous familial hypercholesterolemia (HeFH). This subset of ASCVD affects 1 in 250 people in the population alongside patients diagnosed with premature coronary artery disease (CAD). Vere-102 is under evaluation in Phase 1b clinical trials study and is granted fast track designation by the FDA.
Gimeno spoke further on Vere-102’s potential and what the acquisition means for the treatment’s future saying, "VERVE-102 has the potential to be the first in vivo gene editing therapy for broad patient populations and could shift the treatment paradigm for cardiovascular disease from chronic care to one-and-done treatment. Lilly is eager to welcome our Verve colleagues to Lilly and continue the development of these promising potential new medicines aimed at improving outcomes for patients with cardiovascular disease and addressing the significant unmet medical need in this space."2