Welcome to our dedicated page for Eli Lilly & Co. news (Ticker: LLY), a resource for investors and traders seeking the latest updates and insights on Eli Lilly & Co. stock.
Eli Lilly and Company (NYSE: LLY), founded in 1876 by Colonel Eli Lilly, is a global leader in the pharmaceutical industry, headquartered in Indianapolis, Indiana. With operations in 18 countries and products sold in approximately 125 countries, Eli Lilly is dedicated to pioneering life-changing discoveries through innovative drug development. The company focuses on several therapeutic areas including neuroscience, cardiometabolic, cancer, and immunology.
Key products in Eli Lilly’s portfolio include Verzenio for cancer treatment; Jardiance, Trulicity, Humalog, Humulin, Mounjaro, and Zepbound for diabetes management; and Taltz and Olumiant for immunology. The company's recent financial performance has been robust, with Q1 2024 revenues increasing by 26% year-over-year to $8.77 billion, driven by strong sales of Mounjaro and Zepbound.
Eli Lilly continues to expand its manufacturing capabilities to meet growing demand, recently investing $5.3 billion in its Lebanon, Indiana site. This commitment supports the production of key therapies, particularly for chronic diseases like obesity and type 2 diabetes. The company’s innovative endeavors include the development of new treatments such as the once-weekly insulin efsitora alfa, which showed promising results in phase 3 trials for type 2 diabetes.
The company is also advancing its pipeline of oncology treatments with presentations of data on products like Verzenio, Retevmo, olomorasib, and imlunestrant at major medical conferences. Furthermore, Eli Lilly announced a major leadership change with Melissa Seymour joining as Executive Vice President of Global Quality, ensuring the sustained excellence of their product offerings.
Eli Lilly’s commitment to addressing significant health challenges is evident in its diverse product pipeline and ongoing clinical trials. The company remains focused on improving patient outcomes globally by harnessing advancements in biotechnology, chemistry, and genetic medicine.
Loxo Oncology at Lilly announced the publication of data from the pirtobrutinib (LOXO-305) global Phase 1/2 BRUIN clinical trial in relapsed chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), and other non-Hodgkin lymphomas. Published in The Lancet, findings from the trial demonstrate safety and efficacy across 323 patients. The company plans to initiate four global Phase 3 studies in 2021 to further advance pirtobrutinib’s development, addressing unmet therapeutic needs in patients previously treated with standard care options.
Tirzepatide, from Eli Lilly (NYSE: LLY), demonstrated superior reductions in A1C and body weight compared to semaglutide in the 40-week SURPASS-2 trial involving 1,879 adults with type 2 diabetes. The 15 mg dose of tirzepatide achieved a 2.46% reduction in A1C and a weight loss of 12.4 kg. Notably, 51% of participants on 15 mg reached an A1C below 5.7%, outpacing semaglutide's 20%. Safety profiles were similar, primarily showing gastrointestinal-related adverse events. These results indicate the potential of tirzepatide as a leading treatment option for managing type 2 diabetes.
Eli Lilly and Company and Incyte announced positive top-line results from the BRAVE-AA2 Phase 3 trial for baricitinib in treating severe alopecia areata (AA). Both 2-mg and 4-mg doses showed statistically significant scalp hair regrowth at Week 36 compared to placebo. Baricitinib, designated as Breakthrough Therapy by the FDA, aims to address the unmet needs of AA patients, with no current FDA-approved treatments available. The trial involved 546 diverse participants, with no reported severe adverse events. Detailed results will be presented at upcoming conferences.
The U.S. government has purchased a minimum of 100,000 doses of bamlanivimab (LY-CoV555) and etesevimab (LY-CoV016) from Eli Lilly for $210 million to treat mild to moderate COVID-19 in high-risk patients. This follows their emergency use authorization for such treatments. Additional doses may be purchased, totaling up to 1,200,000 units under certain conditions. The NIH recommends these antibodies to help reduce severe COVID-19 cases. The purchase is part of Lilly's ongoing efforts to combat COVID-19 with their neutralizing antibodies.
Welldoc and Eli Lilly have announced a collaboration to integrate Welldoc's BlueStar software into Lilly's connected insulin solutions. This partnership aims to develop an updated version of the BlueStar app, which will include insulin dosing data from multiple Lilly insulins. The app, FDA-cleared for diabetes management, supports insulin titration and integrates monitoring tools. Lilly plans to submit regulatory approvals in 2021 and commercialize the platform in the U.S. This collaboration seeks to enhance diabetes care through innovative technology.
Eli Lilly and Company (NYSE: LLY) will participate in the Cowen and Company 41st Annual Health Care Conference on March 4, 2021, at 9:10 a.m. Eastern Time. Chief Scientific Officer Daniel Skovronsky will engage in a fireside chat during the event. Investors and media can access a live audio webcast through Lilly's Investor website, with a replay available for approximately 90 days post-event. Lilly continues its commitment to healthcare innovation, focusing on developing life-changing medicines for global communities.
Eli Lilly and Rigel Pharmaceuticals have announced a global exclusive license agreement to co-develop Rigel's RIPK1 inhibitor, R552, targeting autoimmune and inflammatory diseases. Lilly will make an upfront payment of $125 million and could pay up to $835 million in milestone payments, plus royalties. R552 has completed Phase 1 trials and will enter Phase 2 trials in 2021. Lilly will lead clinical development and commercialization efforts, while Rigel retains co-commercialization rights in the U.S. This partnership seeks to advance treatments in both immune and CNS disease areas.
Eli Lilly and Company's tirzepatide demonstrated significant reductions in A1C levels and body weight in phase 3 clinical trials SURPASS-3 and SURPASS-5 for adult patients with type 2 diabetes. After 52 weeks and 40 weeks, respectively, significant endpoints were achieved, with the highest dose (15 mg) lowering A1C by up to 2.59% and body weight by 12.9 kg. Up to 62.4% of participants achieved A1C levels below 5.7%. The safety profile was comparable to existing GLP-1 receptor agonists, with gastrointestinal issues being the most frequent side effects. Results will be presented at upcoming scientific sessions.
On February 16, 2021, Eli Lilly and Company (NYSE: LLY) appointed Kimberly H. Johnson to its board of directors. Johnson, currently the executive vice president and COO of Fannie Mae, will contribute her expertise in technology, governance, and global risk management. She holds degrees in Economics from Princeton University and an MBA from Columbia Business School. Her addition is expected to enhance the board's capabilities, particularly in financial strategy and oversight.
Eli Lilly and Company (NYSE:LLY) announced its participation in the 10th Annual SVB Leerink Global Healthcare Conference on February 24, 2021. Senior Vice President Ilya Yuffa will engage in a fireside chat at 1:40 p.m. ET. A live audio webcast will be accessible on Lilly's investor website, with a replay available for 90 days. Founded over a century ago, Lilly remains committed to producing high-quality medicines and enhancing disease management globally.
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