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AbbVie Inc. (NYSE: ABBV), headquartered in North Chicago, Illinois, is a leading pharmaceutical company ranked 6th on the list of largest biomedical companies by revenue. Known for their commitment to delivering innovative medicines, AbbVie focuses on several key therapeutic areas including immunology, oncology, neuroscience, and eye care. Their portfolio also includes products and services in aesthetics through Allergan Aesthetics, a company they acquired in 2020.
AbbVie’s flagship product, Humira (adalimumab), generated $21 billion in revenue in 2022, accounting for 37% of the company's total revenues. Humira is approved for the treatment of various autoimmune diseases such as rheumatoid arthritis, Crohn's disease, plaque psoriasis, and ulcerative colitis. Beyond Humira, AbbVie has developed other notable immunology drugs, including Skyrizi and Rinvoq, which have shown strong market performance.
In the oncology sector, AbbVie markets Imbruvica and Venclexta, which are critical in treating hematological malignancies. The acquisition of Allergan also brought in new products in aesthetics, including Botox, which is not only a cosmetic treatment but also used therapeutically for various conditions.
AbbVie's research and development efforts are robust, with numerous clinical trials ongoing across its therapeutic areas. Recent achievements include positive topline results from the LEVEL UP study, which demonstrated the efficacy of Rinvoq in treating atopic dermatitis. Financially, AbbVie continues to perform well, reporting first-quarter 2024 revenues of $12.310 billion, a 0.7% increase from the previous year.
Strategic partnerships are also a cornerstone of AbbVie’s growth strategy. Recent collaborations include an agreement with Gilgamesh Pharmaceuticals to develop neuroplastogens for psychiatric disorders and a partnership with Landos Biopharma to enhance their immunology portfolio.
AbbVie remains focused on its mission to address serious health issues and improve patient outcomes globally, leveraging its comprehensive pipeline and innovative solutions in biomedical research.
AbbVie (NYSE: ABBV) has received Breakthrough Therapy Designation (BTD) from the FDA for its investigational drug telisotuzumab vedotin (Teliso-V). This designation targets patients with advanced/metastatic non-small cell lung cancer (NSCLC) characterized by high c-Met overexpression and disease progression post-platinum therapy. Teliso-V aims to address the significant unmet medical needs in NSCLC treatments. Data from the ongoing Phase 2 study (LUMINOSITY) shows promising preliminary efficacy, with an overall response rate of 53.8% among patients with c-Met overexpressing tumors.
AbbVie (NYSE: ABBV) is set to participate in the 40th Annual J.P. Morgan Healthcare Conference on January 11, 2022, at 2:45 p.m. CT. Key executives, including Robert A. Michael, Michael E. Severino, M.D., and Jeffrey R. Stewart, will present virtually. A live audio webcast will be accessible on AbbVie's Investor Relations website, with an archived session available later that day. AbbVie focuses on innovative medicines across various therapeutic areas including immunology and oncology.
On December 16, 2021, Allergan Aesthetics, part of AbbVie (NYSE: ABBV), completed its acquisition of Soliton, Inc. (NASDAQ: SOLY). This acquisition enhances Allergan's offering of non-invasive body contouring solutions by adding the RESONIC™ device, which is FDA-cleared for long-term cellulite improvement and tattoo removal. Clinical data showed that 97.6% of participants reported significant cellulite improvement post-treatment. The acquisition reflects Allergan's commitment to innovation in aesthetic treatments, addressing consumer concerns about cellulite.
AbbVie announced the FDA's approval of RINVOQ (upadacitinib) for treating adults with active psoriatic arthritis (PsA) who are unresponsive or intolerant to TNF blockers. This approval is backed by two Phase 3 trials, SELECT-PsA 1 and SELECT-PsA 2, where RINVOQ met its primary endpoint with ACR20 responses of 71% and 57% vs. placebo. It demonstrated significant improvements in joint efficacy, physical function, and fatigue. Despite its benefits, RINVOQ carries risks of serious infections and cardiovascular events, particularly in older patients with heart disease risk factors.
Allergan, part of AbbVie, announced the availability of VUITY™ (pilocarpine HCl ophthalmic solution) 1.25%, the first FDA-approved eye drop for treating presbyopia, affecting around 128 million Americans. The innovative formulation utilizes proprietary pHast™ technology to enhance near vision while maintaining distance focus. Clinical studies demonstrated significant efficacy, with participants achieving notable improvements in visual acuity.
VUITY is now available by prescription in pharmacies across the U.S., emphasizing AbbVie's commitment to advancing eye care.
AbbVie announced promising top-line results from the Phase 3 U-EXCEED study of upadacitinib for moderate to severe Crohn's disease. At week 12, 39% of patients achieved clinical remission via CDAI, and 40% showed remission via SF/AP, significantly outperforming the placebo (21% and 14%, respectively; p<0.0001). Endoscopic response was seen in 35% of the upadacitinib group versus 4% in placebo (p<0.0001). The safety profile remains consistent with previous studies, with common adverse events predominantly mild. Full data will be presented at medical conferences soon.
AbbVie has updated the U.S. prescribing information for RINVOQ (upadacitinib) for moderate to severe rheumatoid arthritis (RA) treatment. This follows an FDA Drug Safety Communication on Sept. 1, 2021, which flagged risks like malignancy and major adverse cardiac events (MACE) associated with JAK inhibitors. The updated label now emphasizes these risks in the warnings section. RINVOQ is now indicated for patients with an inadequate response or intolerance to TNF blockers. The FDA is also reviewing supplemental applications for RINVOQ for several additional conditions.
AbbVie has submitted an application to the European Medicines Agency (EMA) for risankizumab (SKYRIZI) as a treatment for moderate to severe active Crohn's disease in patients aged 16 and older. This application is based on results from three pivotal Phase 3 studies: ADVANCE, MOTIVATE, and FORTIFY, which demonstrated significant improvements in clinical remission and endoscopic response. No new safety risks were identified compared to the existing safety profile. Approval is still pending, and risankizumab's use for Crohn's disease has not yet been established by regulatory authorities.
AbbVie (NYSE: ABBV) will participate in the 4th Annual Evercore ISI Virtual HealthCONx Conference on December 2, 2021, at 11:10 a.m. CT. Key executives, including Michael Severino, Robert A. Michael, and Jeffrey R. Stewart, will present. A live audio webcast will be available on AbbVie’s Investor Relations website, with an archived edition accessible later that day. AbbVie aims to discover innovative medicines to address serious health issues across various therapeutic areas, including immunology and oncology.
AbbVie (NYSE: ABBV) will participate in the Piper Sandler 33rd Annual Virtual Healthcare Conference on December 1, 2021, at 9:30 a.m. CT. Key executives, including Michael Severino, Robert A. Michael, and Jeffrey R. Stewart, will present during the event. The presentation can be accessed via a live audio webcast on AbbVie's Investor Relations website, with an archived version available later that day. AbbVie is dedicated to discovering innovative treatments across various therapeutic areas, including immunology, oncology, and neuroscience.
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