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.
Eli Lilly (NYSE: LLY) announced that the FDA has granted Emergency Use Authorization (EUA) for its monoclonal antibody, bebtelovimab, to treat mild-to-moderate COVID-19 in high-risk adults and pediatric patients. The treatment is authorized for patients with positive SARS-CoV-2 tests who lack suitable alternatives. The recommended dose is 175 mg via intravenous injection. Eli Lilly has secured a supply agreement with the U.S. government for 600,000 doses, valued at approximately $720 million. Bebtelovimab retains efficacy against Omicron and other variants of concern.
Eli Lilly and Company (NYSE: LLY) announced a contract with the U.S. government to supply up to 600,000 doses of the investigational COVID-19 treatment, bebtelovimab, for at least $720 million. The agreement is contingent on the drug receiving Emergency Use Authorization (EUA) from the FDA, a request that has been submitted. The projected revenue impact for 2022 is at least $720 million, with an estimated $0.20 in earnings per share (EPS). Bebtelovimab demonstrates strong efficacy against COVID-19 variants, maintaining full neutralizing activity against Omicron and other variants of concern.
Eli Lilly and Company (NYSE: LLY) has appointed Cynthia Cardona as president of the Eli Lilly and Company Foundation and senior director of social impact. Cardona will lead initiatives focused on racial justice, education, and global health. With experience dating back to 2001, she has held various leadership roles within the company, including chief marketing officer for Lilly Japan. The Foundation, established in 1968, aims to improve health and educational opportunities while addressing racial inequities. Forward-looking statements in the PR highlight potential risks linked to leadership changes.
Eli Lilly and Company (LLY) reported strong financial results for Q4 and the full year 2021, showcasing an 8% revenue increase in Q4 to $8 billion and a 15% annual growth to $28.3 billion. The company highlighted significant growth in key products, including Trulicity and Taltz. However, net income decreased by 18% in Q4 and 10% for the year, primarily due to reduced other income and increased operating expenses. Lilly continues to pursue an exciting pipeline and expects 2022 EPS in the range of $8.00 to $8.15, affirming confidence in future growth.
Eli Lilly and Company (NYSE: LLY) has partnered with UNICEF to improve health outcomes for 10 million children and adolescents suffering from chronic non-communicable diseases (NCDs) by 2025. Lilly will contribute $14.4 million to enhance healthcare systems and support health workers in Bangladesh, Malawi, Nepal, the Philippines, and Zimbabwe. This collaboration aims to combat diseases like diabetes and cancer, addressing the crisis where nearly one million children under 20 die annually due to often treatable conditions.
Eli Lilly and Company (NYSE: LLY) will participate in the Guggenheim Oncology Conference on February 9, 2022. Key figures, including Jake Van Naarden, CEO of Loxo Oncology at Lilly, and David Hyman, M.D., Chief Medical Officer of Lilly Oncology, will engage in a virtual fireside chat at 12 p.m. Eastern time. Investors can access a live audio webcast through Lilly's Investor website, with a replay available for approximately 90 days thereafter. Eli Lilly remains committed to discovering life-changing medicines and giving back to communities.
Eagle Pharmaceuticals has launched PEMFEXY (pemetrexed for injection), a new treatment for nonsquamous non-small cell lung cancer and mesothelioma. Sales started today, following FDA approval and a settlement with Eli Lilly. The U.S. market for ALIMTA, a competitor, reached
Eli Lilly plans to invest over $1 billion in a new manufacturing site in Concord, North Carolina, creating nearly 600 new jobs. This facility aims to enhance manufacturing capacity for injectable products and leverage advanced technology. The decision reflects Lilly's commitment to growth in the pharmaceutical sector and its ongoing investments in North Carolina, totaling over $4 billion in the past five years. The investment is contingent on local government approvals, and an additional $500 million will be spent on a biopharmaceutical facility in Ireland.
Eli Lilly and Incyte provided updates on the Phase 3 development for OLUMIANT (baricitinib) in systemic lupus erythematosus (SLE) and atopic dermatitis. The Phase 3 lupus program has been discontinued after the SLE-BRAVE-I study met its primary endpoint, while SLE-BRAVE-II did not. Ongoing discussions with the FDA may lead to a Complete Response Letter for the atopic dermatitis sNDA due to lack of alignment on the indicated population. Lilly remains committed to other research with OLUMIANT, including potential regulatory approvals for COVID-19 and alopecia areata in 2022.
Eli Lilly and Company (NYSE: LLY) will announce its fourth-quarter and full-year 2021 financial results on February 3, 2022. A conference call is scheduled for 9 a.m. Eastern time on the same day, accessible via a live webcast on Lilly's website. The call will provide detailed insights into the company's financial performance for the year. Investors and the public are invited to participate, and a replay will be available afterward.
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