Welcome to our dedicated page for Abbvie news (Ticker: ABBV), a resource for investors and traders seeking the latest updates and insights on Abbvie stock.
AbbVie Inc. (ABBV) is a global biopharmaceutical leader driving innovation in immunology, oncology, and neuroscience therapies. This page provides real-time access to AbbVie's official press releases, regulatory milestones, and strategic developments.
Investors and industry professionals will find a curated collection of earnings reports, FDA approval updates, clinical trial results, and partnership announcements. Our comprehensive resource eliminates the need to track multiple sources, offering verified information directly from corporate communications and trusted financial publications.
Key content includes updates on AbbVie's R&D pipeline, mergers & acquisitions like the Allergan integration, patent developments, and market expansion initiatives. All materials are organized chronologically for efficient analysis of the company's trajectory.
Bookmark this page for streamlined monitoring of AbbVie's operational and financial performance. Check back regularly to stay informed about developments impacting one of the pharmaceutical sector's most influential innovators.
AbbVie (NYSE: ABBV) has completed its acquisition of Cerevel Therapeutics (NASDAQ: CERE), strengthening its neuroscience portfolio. The acquisition brings multiple clinical-stage assets, including emraclidine, a potential best-in-class antipsychotic for schizophrenia, and tavapadon, a first-in-class treatment for Parkinson's disease. AbbVie expects the acquisition to be accretive to adjusted diluted EPS beginning in 2030.
The company reaffirms its 2024 full-year adjusted diluted EPS guidance range of $10.71-$10.91, which includes a $0.19 per share dilutive impact from the Cerevel acquisition. AbbVie also maintains its third-quarter adjusted diluted EPS guidance range of $2.92-$2.96. The acquisition is expected to contribute to AbbVie's long-term performance and complement its existing neuroscience pipeline.
Allergan Aesthetics, an AbbVie company (NYSE: ABBV), announces the return of JUVÉDERM® Day on August 21, 2024. This second annual event offers exclusive deals and savings through the Allē loyalty program. Highlights include:
1. BOGO Gift Cards: Members can purchase a $75 JUVÉDERM® gift card and receive an additional $75 card free.
2. Allē Flash: Schedule a consultation for a chance to save up to $500 on JUVÉDERM® treatment.
3. Sweepstakes: Get treated by September 30 for a chance to win $10,000.
JUVÉDERM® remains the top chosen hyaluronic acid dermal filler collection globally. The event aims to surpass last year's record-breaking treatment numbers and drive consumers to practices. Allē, serving over 7 million members across ~30,000 practices, offers rewards on various aesthetic treatments and flexible payment plans.
AbbVie (NYSE: ABBV) announced that the European Commission has approved SKYRIZI® (risankizumab) for treating adult patients with moderately to severely active ulcerative colitis (UC). This marks SKYRIZI's fourth approved indication in the European Union. The approval is based on data from two Phase 3 trials: INSPIRE (induction) and COMMAND (maintenance).
Key findings include:
- In INSPIRE, 20% of patients achieved clinical remission at week 12 with SKYRIZI vs 6% with placebo
- In COMMAND, 40% and 38% of patients achieved clinical remission at week 52 with SKYRIZI 180mg and 360mg, respectively, vs 25% in the control group
- Significant improvements in mucosal healing were observed, especially in patients without previous biologic or JAK inhibitor failure
The safety profile was consistent with previous trials, with no new safety risks identified.
AbbVie (NYSE:ABBV) reported Q2 2024 financial results with net revenues of $14.462 billion, up 4.3% on a reported basis. Diluted EPS was $0.77 on a GAAP basis, down 32.5%, while adjusted diluted EPS was $2.65, down 8.9%. Key highlights include:
- Immunology portfolio revenues: $6.971 billion, up 2.3%
- Oncology portfolio revenues: $1.634 billion, up 10.5%
- Neuroscience portfolio revenues: $2.162 billion, up 14.7%
- Aesthetics portfolio revenues: $1.390 billion, up 0.5%
AbbVie raised its 2024 adjusted diluted EPS guidance to $10.71 - $10.91. The company also announced leadership changes, with Robert A. Michael assuming the role of CEO effective July 1, 2024.
AbbVie has submitted regulatory applications to the FDA and EMA for upadacitinib (RINVOQ®) to treat giant cell arteritis (GCA). This autoimmune disease affects medium and large arteries, causing symptoms such as headaches, jaw pain, and vision changes, potentially leading to permanent vision loss. The applications are backed by Phase 3 SELECT-GCA study results, showing that upadacitinib (15 mg once daily) with a 26-week steroid taper regimen achieved sustained remission from week 12 through 52. The safety profile was consistent with existing conditions treated by upadacitinib.
AbbVie (NYSE:ABBV) has appointed Roopal Thakkar, M.D., as Executive Vice President, Research & Development, and Chief Scientific Officer. Thakkar, who is currently the Senior Vice President and Chief Medical Officer, Global Therapeutics, will now lead AbbVie's global R&D division, encompassing over 14,000 members across all discovery and development stages, including therapeutics and aesthetics. CEO Rob Michael highlighted Thakkar's robust track record in forging strategic partnerships and advancing clinical programs. Thomas J. Hudson, M.D., who served as Chief Scientific Officer since 2019, will retire. Hudson has been instrumental in shaping AbbVie's early-stage science and precision medicine capabilities since joining in 2016.
AbbVie (NYSE: ABBV) is set to release its second-quarter 2024 financial results on Thursday, July 25, 2024, before the market opens. The company will hold a live webcast of the earnings conference call at 8 a.m. Central time, accessible through its Investor Relations website. Additionally, an archived edition of the session will be made available later the same day.
AbbVie announced that Robert A. Michael has assumed the role of Chief Executive Officer (CEO) and joined the Board of Directors effective July 1, 2024. Michael succeeds Richard A. Gonzalez, who will now serve as Executive Chairman. Michael, with over 31 years of experience, previously held roles including President and Chief Operating Officer, Vice Chairman, and Chief Financial Officer. He will lead AbbVie with a focus on innovation and growth.
Gonzalez expressed confidence in Michael's leadership, highlighting a strong leadership team and a solid financial foundation for AbbVie's future. Michael emphasized his commitment to AbbVie's mission and thanked Gonzalez for his leadership.
AbbVie has received a positive opinion from the European Medicines Agency's CHMP for epcoritamab (TEPKINLY®), a bispecific antibody for treating adults with relapsed/refractory follicular lymphoma (R/R FL) after two or more prior therapies. If approved, it will be the first bispecific antibody conditionally approved for both R/R FL and R/R diffuse large B-cell lymphoma (DLBCL) in the EU. This recommendation is based on results from the Phase 1/2 EPCORE® NHL-1 study, which showed significant overall and complete response rates. The European Commission's decision is expected later this year. Follicular lymphoma accounts for 20-30% of all non-Hodgkin's lymphoma cases, with about 13,000 cases in Western Europe in 2023. The collaboration between AbbVie and Genmab aims to secure additional international regulatory approvals.
AbbVie (NYSE: ABBV) announced the acquisition of Celsius Therapeutics, a biotechnology company focused on inflammatory diseases. This $250 million cash deal includes adjustments and aims to advance Celsius' leading investigational asset, CEL383, an anti-TREM1 antibody for treating inflammatory bowel disease (IBD). CEL383 has completed Phase 1 clinical trials and targets TREM1, a gene linked to inflammation in IBD. AbbVie believes CEL383 could help more IBD patients achieve remission, reflecting the company's commitment to expanding its immunology portfolio.