Welcome to our dedicated page for Abbott Labs news (Ticker: ABT), a resource for investors and traders seeking the latest updates and insights on Abbott Labs stock.
Abbott Laboratories (NYSE: ABT) generates a steady flow of news across diagnostics, medical devices, nutritionals and branded generic medicines, reflecting its role as a global healthcare company serving people in more than 160 countries. News coverage on this page highlights regulatory milestones, product launches, clinical data, corporate actions and community initiatives that shape Abbott’s business and its impact on patients.
Recent announcements include FDA approvals and clearances for cardiovascular and structural heart technologies, such as the Volt PFA System for treating atrial fibrillation and the Amplatzer Piccolo Delivery System for minimally invasive closure of patent ductus arteriosus in premature infants. Abbott also reports developments in diabetes care and metabolic health, including enhancements to its Libre app through the Libre Assist feature, which uses generative AI and continuous glucose monitoring data to help people living with diabetes understand how food choices may affect glucose levels, and the expansion of its Lingo over-the-counter continuous glucose monitor to additional mobile platforms.
Investors and observers will also find news about Abbott’s nutrition business, such as new Ensure Max Protein shakes aimed at supporting muscle health for active and older adults, as well as information on public health partnerships and community programs like the "We Give Blood" competition with the Big Ten Conference and the HeartMates community for people with heart health challenges. Corporate updates include dividend declarations and increases, as well as the announced Agreement and Plan of Merger to acquire Exact Sciences Corporation, which would expand Abbott’s presence in cancer screening and precision oncology diagnostics.
This news feed provides a centralized view of Abbott’s latest announcements, allowing readers to follow developments in its key business segments and understand how new products, regulatory events and strategic transactions may influence the company over time.
Abbott has received FDA clearance for its Alinity™ m STI Assay, a multiplex test capable of detecting four sexually transmitted infections (STIs) simultaneously: Chlamydia, Gonorrhea, Trichomonas, and Mycoplasma. The test addresses rising STI rates exacerbated by pandemic-related disruptions in routine testing. Utilizing the advanced Alinity m system, this test enhances efficiency in diagnosis and treatment for healthcare providers. Abbott aims to improve accessibility to STI testing, reflecting on the changes in healthcare delivery during the pandemic.
Abbott (NYSE: ABT) is releasing limited quantities of metabolic nutrition formulas at the U.S. FDA's request, following a recall of some infant formulas. The released products were not part of the February recall and have met safety standards. Patients can obtain these formulas through healthcare providers and referrals. Abbott's Sturgis facility remains under scrutiny, but no link has been found between it and reported infant illnesses. The company is working with the FDA to resume operations, with new production expected in six to eight weeks.
Abbott's PERSIST-END study revealed that 89% of patients with persistent atrial fibrillation (AFib) treated with the TactiCath™ Contact Force Ablation Catheter remained symptom-free for up to 15 months. The study, involving 224 patients, showed significant improvements in quality of life scores and a 53% reduction in healthcare resource utilization post-procedure. Conducted from 2018-2021, the trial met its primary safety and efficacy endpoints, indicating TactiCath SE's effectiveness in managing persistent AFib and enhancing patient outcomes.
Abbott (NYSE: ABT) has launched the Amplatzer™ Steerable Delivery Sheath in the U.S. to assist in sealing the left atrial appendage (LAA) for patients with atrial fibrillation at risk of stroke. This first-of-its-kind system enhances precision and flexibility during procedures using the Amplatzer Amulet™ LAA Occluder, which aims to reduce stroke risk without long-term blood-thinning medications. The sheath features bi-directional steering, an auto-lock function, and a valve to stabilize blood flow, reinforcing Abbott's commitment to innovation in structural heart therapies.
Abbott (NYSE: ABT) announced results from a meta-analysis of 75 studies indicating its FreeStyle Libre system significantly reduces glycated hemoglobin (HbA1c) in adults with type 1 and type 2 diabetes. After three months, HbA1c levels decreased by 0.53% for type 1 and 0.45% for type 2 diabetes, with reductions sustained for up to 24 months for type 1 and 12 months for type 2. The findings highlight the importance of access to glucose monitoring technology for insulin-using individuals with type 2 diabetes, as it provides similar benefits to those with type 1.
On April 27, 2022, Abbott, CamDiab, and Ypsomed announced a partnership to develop an integrated automated insulin delivery (AID) system targeting diabetes management. This innovative system will combine Abbott's FreeStyle Libre 3 sensor, CamDiab's CamAPS FX algorithm, and Ypsomed's mylife YpsoPump. By enhancing glucose monitoring and insulin delivery, the trio aims to improve health outcomes for diabetes patients, particularly in Europe. Development is expected to conclude by the end of 2022, with commercialization anticipated to follow shortly after.
Abbott (NYSE: ABT) announced its rejection of an unsolicited mini-tender offer by TRC Capital Investment Corporation to buy up to 1,000,000 shares at $112.38 each, which is about 4.5% below Abbott's closing price of $117.69 on April 14, 2022. Abbott advises shareholders not to tender their shares, emphasizing the offer price is significantly lower than market value. Shareholders are encouraged to consult with financial advisors and take caution regarding TRC's offer, which is set to expire on May 17, 2022. Abbott is not associated with TRC and urges the withdrawal of any shares tendered.
Abbott has launched an upgraded version of its NeuroSphere myPath digital health app, enhancing its functionality for tracking pain relief during treatment with neurostimulation devices. Available for both Apple and Android, the app facilitates better communication between doctors and patients, enabling a shared view of patient-reported outcomes. Chronic pain affects over 50 million Americans, and the app aims to personalize treatment by allowing patients to document pain levels and overall well-being throughout their therapy journey.
Abbott reported Q1 2022 sales of $11.9 billion, reflecting a 13.8% increase year-over-year, with organic growth at 17.5%. COVID-19 testing-related sales reached $3.3 billion. Excluding these, reported sales grew 3.9%, and organic sales grew 7.7%. GAAP diluted EPS rose by 37.0% to $1.37, while adjusted EPS grew 31.1% to $1.73. Notable developments include FDA approvals for new products, although Nutrition sales decreased, impacted by a voluntary recall.
Abbott has received FDA approval for its Aveir™ single-chamber (VR) leadless pacemaker, designed for patients with slow heart rhythms. This innovation, the world's only leadless pacemaker with unique mapping capability, allows physicians to assess device positioning before implantation. With a projected battery life up to twice as long as competitors, it can also be retrieved for therapy adjustments. The approval comes after successful results from the global LEADLESS II study. This device marks a significant advancement in cardiac care, minimizing complications associated with traditional pacemakers.