Welcome to our dedicated page for Lilly Eli & Co news (Ticker: LLY), a resource for investors and traders seeking the latest updates and insights on Lilly Eli & Co stock.
Eli Lilly and Company (NYSE: LLY) generates frequent news across cardiometabolic health, oncology, immunology, obesity and manufacturing expansion. This page aggregates recent press releases and third-party coverage so readers can follow how Lilly’s medicines, clinical programs and corporate actions are evolving over time.
Recent updates show Lilly reporting Phase 3 results for multiple late-stage assets. In obesity and cardiometabolic health, the company has shared topline data from ATTAIN-MAINTAIN, a Phase 3 trial of orforglipron, an investigational once-daily oral GLP-1 receptor agonist, for weight maintenance after prior treatment with injectable incretin therapies. Lilly has also reported results from TRIUMPH-4, a Phase 3 trial of retatrutide, an investigational triple agonist targeting GIP, GLP-1 and glucagon receptors, in adults with obesity or overweight and knee osteoarthritis, with co-primary endpoints in weight loss and pain reduction.
In immunology, Lilly has announced positive topline results from the TOGETHER-PsA Phase 3b trial, which evaluated concomitant use of Taltz (ixekizumab) and Zepbound (tirzepatide) versus Taltz alone in adults with active psoriatic arthritis and obesity or overweight with at least one weight-related condition. The company reports that the combination met the primary endpoint and all key secondary endpoints, supporting an integrated approach to treating psoriatic arthritis and obesity.
Oncology news includes updated EMBER-3 data for Inluriyo (imlunestrant) as monotherapy and in combination with Verzenio (abemaciclib) in ER-positive, HER2-negative advanced breast cancer, and Phase 3 BRUIN CLL-313 results showing that Jaypirca (pirtobrutinib) significantly reduced the risk of progression or death versus chemoimmunotherapy in treatment-naïve CLL/SLL without 17p deletions.
Corporate and strategic news items cover Lilly’s planned acquisition of Ventyx Biosciences, completion of the Adverum Biotechnologies tender offer, a strategic collaboration with Aktis Oncology, and a major manufacturing investment in a new active pharmaceutical ingredient facility in Huntsville, Alabama. Investors and observers can use this news feed to monitor clinical milestones, regulatory submissions, acquisitions, collaborations, financing activities and manufacturing expansions related to LLY.
Eli Lilly's Phase 3 LUCENT-2 study on mirikizumab shows that 50% of ulcerative colitis patients achieved clinical remission after one year, with almost all not using steroids. The drug outperformed placebo across all key endpoints, with 63.6% maintaining remission. Patients reported significant reductions in bowel urgency severity, and adverse events were lower compared to placebo. Lilly seeks regulatory approvals in the US and EU in 2023, potentially positioning mirikizumab as the first anti-IL23p19 treatment for ulcerative colitis.
Eli Lilly and Company (NYSE: LLY) is hosting a webcast on June 7, 2022, at 11:30 a.m. ET, discussing its diabetes and obesity portfolio. Key topics include results from the tirzepatide SURMOUNT-1 clinical trial and details on Lilly's weekly basal insulin and early-phase incretins. The event will be accessible via the company's Investor website, with a replay available for 90 days following the event. Lilly aims to advance healthcare solutions addressing significant health challenges, including diabetes and obesity.
Eli Lilly and Incyte announced a positive opinion from the European Medicines Agency's CHMP for OLUMIANT (baricitinib) to treat adults with severe alopecia areata. This opinion signals the potential for the first oral treatment and JAK inhibitor for severe alopecia areata in the EU, pending final approval from the European Commission, expected in the next 1-2 months. The judgment is based on the successful Phase 3 BRAVE-AA1 and BRAVE-AA2 trials, involving 1,200 patients, showing significant efficacy compared to placebo. The FDA has granted priority review for the same indication in the U.S.
Eli Lilly and Company (NYSE: LLY) will participate in the UBS Global Healthcare Conference on May 24, 2022, at 8:30 a.m. ET. Michael Mason, the Senior Vice President and President of Lilly Diabetes, will engage in a fireside chat at the event. A live audio webcast of this presentation will be accessible on Lilly's Investor website, with a replay available for 90 days. Lilly focuses on advancing healthcare solutions, impacting over 47 million people globally through innovative therapies targeting major health challenges. For more details, visit Lilly.com.
The FDA has approved Mounjaro (tirzepatide) for adults with type 2 diabetes, marking it as the first GIP and GLP-1 receptor agonist. Mounjaro is set to provide significant A1C reductions of 1.7% to 2.4% and promote weight loss, with average reductions ranging from 12 to 25 lbs. in clinical trials. It will be available in the U.S. in multiple doses. Side effects include nausea and a boxed warning for thyroid tumors. Lilly aims to enhance access through partnerships with insurers and plans to offer savings cards to eligible patients.
The FDA has approved OLUMIANT (baricitinib), marking it as the first and only JAK inhibitor authorized for treating hospitalized adults with COVID-19 requiring oxygen support. Recommended dosing is 4 mg once daily for up to 14 days. This approval is based on positive results from Phase 3 studies ACTT-2 and COV-BARRIER, where OLUMIANT showed effectiveness without new safety concerns. Approximately one million patients have already received OLUMIANT globally since its emergency use in November 2020. Caution is advised due to risks of serious infections and other severe adverse events.
Eli Lilly and Company (NYSE: LLY) has elected Dr. Mary Lynne Hedley to its Board of Directors, effective May 15, 2022. Dr. Hedley, an expert in immunology and oncology, brings extensive experience from her roles at the Broad Institute and TESARO, a biotech firm she co-founded. She will serve on the Science & Technology Committee and the Ethics and Compliance Committee. CEO David A. Ricks expressed optimism about her addition, highlighting her leadership and technological insights as vital to Lilly's ongoing innovation and growth in the pharmaceutical industry.
Eli Lilly and Company (NYSE: LLY) will attend the Bank of America Securities 2022 Healthcare Conference on May 10-11, 2022. Daniel Skovronsky, M.D., Ph.D., will participate in a fireside chat on May 10 at 7:40 p.m. ET. A live audio webcast will be accessible on Lilly's Investor website, with a replay available for 90 days. Lilly aims to advance health through innovative therapies, impacting over 47 million people worldwide. For more details, visit Lilly's Investor site.
Eli Lilly and Company (NYSE: LLY) has declared a $0.98 dividend per share for the second quarter of 2022. This dividend is payable on June 10, 2022, to shareholders of record by May 16, 2022. The company focuses on innovative treatments for significant health challenges impacting millions globally. Lilly’s commitment includes enhancing accessibility and affordability of its medicines, and it has been pioneering advancements for nearly 150 years.
IgGenix, a biotechnology firm focused on alleviating allergic diseases, announces its move to Lilly Gateway Labs in South San Francisco, CA. This relocation aims to foster collaborations for scientific breakthroughs in allergy treatments. With over 50 million affected by allergies in the U.S., IgGenix intends to leverage its innovative single-cell discovery platform to develop safer therapeutic options. This partnership is expected to enhance access to Lilly's resources and expertise, ultimately addressing unmet treatment needs in the allergy space.