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. (NYSE: ABBV) is a pharmaceutical preparation manufacturing company that regularly issues news on its medicines, research programs, collaborations and manufacturing plans. Company communications emphasize a mission to discover and deliver medicines and solutions in key therapeutic areas such as immunology, oncology, neuroscience and eye care, as well as offerings in its Allergan Aesthetics portfolio.
News about AbbVie often covers clinical and scientific developments, particularly in oncology and blood cancers. The company has reported new data at major medical meetings, including results for investigational agents like etentamig (ABBV‑383) and PVEK, and updates on approved medicines such as EPKINLY (epcoritamab-bysp) and VENCLEXTA (venetoclax). Releases may detail trial outcomes, regulatory milestones, and additional indications under investigation.
Investors and observers can also find corporate and financial updates in AbbVie’s news flow, including announcements of earnings conference calls, participation in healthcare and investor conferences, and guidance-related information that aligns with its SEC filings. The company additionally highlights strategic agreements and collaborations, such as its exclusive licensing agreement with RemeGen for the PD‑1/VEGF bispecific antibody RC148 and its voluntary agreement with the U.S. administration focused on access, affordability and U.S.-based investment.
Another recurring theme in AbbVie’s news is manufacturing and investment activity. The company has announced a definitive agreement to acquire a device manufacturing facility in Tempe, Arizona, to expand drug delivery device manufacturing for immunology and neuroscience medicines, and has referenced multi‑year commitments to U.S. R&D and capital investments. AbbVie also publishes stories on patient- and community-focused initiatives, such as the “Second Winds” film about people living with chronic lymphocytic leukemia. For readers tracking ABBV, this news stream provides insight into the company’s research pipeline, regulatory progress, capital allocation and patient engagement efforts.
AbbVie (NYSE: ABBV) submitted an FDA application for upadacitinib (RINVOQ) 15 mg and 30 mg once daily for adults and adolescents with severe alopecia areata, based on Phase 3 UP-AA data.
In two replicate trials (N=1,399), the primary endpoint SALT ≤ 20 at week 24 was met for both doses; response rates improved through week 52. Safety through week 52 was described as consistent with earlier results. Use in AA is not approved and remains under regulatory review.
AbbVie (NYSE: ABBV) submitted an application to the FDA on April 27, 2026, seeking approval for SKYRIZI (risankizumab-rzaa) as a subcutaneous (SC) induction treatment for adults with moderately to severely active Crohn's disease.
The filing is supported by positive Phase 3 AFFIRM study data and would give patients an option between SC induction or the existing IV induction, continuing SC maintenance every eight weeks if approved.
AbbVie (NYSE: ABBV) received a Complete Response Letter (CRL) from the U.S. Food and Drug Administration on April 23, 2026 for its Biologics License Application for trenibotulinumtoxinE (TrenibotE).
The FDA requested additional information about manufacturing processes; the CRL did not identify safety or efficacy concerns and did not request additional clinical studies. AbbVie expects to submit a response in the coming months and says international regulatory reviews are progressing.
AbbVie (NYSE: ABBV) will invest $1.4 billion to build a new 185-acre pharmaceutical manufacturing campus in Durham, North Carolina, supporting production of immunology, neuroscience and oncology medicines.
Construction begins in 2026 with completion expected by end of 2028, creating 734 full-time jobs and more than 2,000 construction jobs, and forming part of AbbVie's $100 billion U.S. R&D and capital commitment.
Allergan Aesthetics (NYSE: ABBV) partnered with entrepreneur Erin Lichy to share her Natrelle® breast augmentation journey on social media, aiming to normalize conversations about aesthetic surgery and support patient education.
The release highlights Natrelle®'s 50-year heritage, a 10-year clinical safety profile, implant options, and a nationwide Faces of Natrelle® testimonial program.
Haisco and AbbVie (NYSE: ABBV) entered an exclusive license agreement announced April 10, 2026, covering multiple pain compounds.
Haisco granted AbbVie global development, manufacturing, and commercialization rights excluding mainland China, Hong Kong, and Macau. Haisco will receive an upfront payment of USD $30 million, up to USD $715 million in milestones, and tiered royalties on future net sales.
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BOTOX Cosmetic (NYSE: ABBV) reopens applications for The Confidence Collective, running through April 29, 2026. The program will provide resources to 250 women entrepreneurs and award twenty $20,000 grants. Since 2023, the brand has awarded $1.2M to grant winners to support business growth and mentorship.
Selected cohort members will receive coaching, community access, and mentoring; grant winners will be announced this fall. Applicants must submit by April 29, 11:59 p.m. PT and agree to program terms.
Allergan Aesthetics (NYSE: ABBV) opened the new Allergan Medical Institute (AMI) Austin on April 7, 2026, its third U.S. AMI Training Center in the past year. The state-of-the-art facility offers immersive, hands-on education across facial injectables, body contouring, skincare, and regenerative medicine to advance clinical proficiency for providers.
AMI Austin emphasizes advanced injection techniques, complication management, practice development, and peer collaboration under Medical Director Dr. Saami Khalifian, supporting the company’s broader training network including Orange County and Atlanta centers.
Allergan Aesthetics (NYSE: ABBV) announced its fourth annual CoolMonth promotion running April 1–30, 2026, offering $400 off first-time CoolSculpting treatments for eligible Allē members and social giveaways up to $5,000.
CoolSculpting and CoolSculpting Elite are FDA-cleared for specific visible fat bulges and submental laxity; they are not weight-loss treatments. Entry and eligibility details apply.