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 reports developments across a global healthcare portfolio that includes diagnostics, medical devices, nutritionals and branded generic medicines. Recurring updates cover cardiovascular technologies such as Ultreon coronary imaging, pulsed field ablation and cardiac pacing systems; diabetes and other medical devices; nutritional products; and diagnostic testing.
Abbott news also includes financial results, guidance, product clearances, clinical data presentations, commercial integrations and portfolio changes. Following the completed Exact Sciences acquisition, oncology diagnostics are a recurring theme, including Cologuard, Oncotype DX, Oncodetect, Riskguard and Cancerguard tests for cancer screening, recurrence risk and treatment support.
Abbott has announced a 25% increase in its quarterly common dividend, raising it to 45 cents per share. This decision reflects Abbott's strong business momentum and commitment to providing immediate value to shareholders. The upcoming dividend, marking the 388th consecutive quarterly payment since 1924, will be distributed on February 16, 2021, to shareholders on record by January 15, 2021. Abbott has maintained a remarkable 49 consecutive years of dividend increases and is listed in the S&P 500 Dividend Aristocrats Index.
Abbott's FreeStyle Libre 2 system has received approval from Health Canada for diabetes management in adults and children aged 4 and older. This innovative glucose monitoring technology includes features like real-time alarms and continuous glucose measurement every minute, sustaining performance for 14 days. It aims to improve diabetes management by providing actionable insights for users and healthcare providers, all at the same price as the original FreeStyle Libre system. The FreeStyle Libre 2 will be accessible to over 3.7 million Canadians living with diabetes.
Abbott has become the first anchor sponsor of the American Diabetes Association's Health Equity Now initiative, committing $5 million over three years. This platform aims to address health disparities faced by underserved diabetes populations. Data highlights that the risk of diabetes is significantly higher among Black Americans (77%) and Latinos (66%). Abbott will support advocacy efforts to enhance access to medical technologies and foster community engagement programs to improve health outcomes among these communities.
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Abbott has launched the IonicRF™ Generator, a radiofrequency ablation device cleared by the FDA for non-surgical pain management targeting the nervous system. This is Abbott's first radiofrequency device, approved in both the U.S. and Europe. Designed to provide a tailored approach for pain relief, studies indicate the therapy can offer relief for 6-12 months. This launch helps expand Abbott's neuromodulation portfolio aimed at patients seeking alternatives to surgery and opioids.
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Abbott reported third-quarter 2020 sales of $8.9 billion, reflecting a 9.6% increase from the previous year. Diluted EPS was $0.69 GAAP and $0.98 adjusted, marking a 16.7% growth. Abbott expects full-year GAAP EPS of at least $2.35 and adjusted EPS of $3.55. Notable developments include FDA Emergency Use Authorization for the BinaxNOW COVID-19 test and the launch of FreeStyle Libre 2. The company maintains a strong dividend history, recently declaring its 387th consecutive quarterly dividend.
Researchers from Abbott, the University of Illinois, and the U.S. Air Force have discovered a strong connection between physical fitness, cognitive performance, and optimal nutrition. In a 12-week study involving 148 U.S. Air Force personnel, participants receiving a high-protein nutritional drink exhibited improvements including an 11% boost in working memory and a 6% enhancement in reaction time. Additionally, muscle mass increased by over two pounds, and resting heart rate dropped by 8%. Abbott aims to develop future nutritional products based on these findings.
Abbott (NYSE: ABT) has received Emergency Use Authorization (EUA) from the FDA for its AdviseDx SARS-CoV-2 IgM lab-based serology test. This test, available on ARCHITECT and Alinity platforms, detects IgM antibodies to indicate recent or prior COVID-19 infections. Abbott has developed seven tests for COVID-19 since the pandemic began, including molecular and rapid antigen tests. The new test demonstrates high reliability with 99.56% specificity and 95.00% sensitivity, aiding healthcare providers in assessing patient recovery.
Abbott has released interim clinical data on its ID NOW COVID-19 rapid test, confirming previous FDA submissions for Emergency Use Authorization. The study involved 1,003 participants and demonstrated an overall performance of 93.3% positive agreement and 98.4% negative agreement to lab-based PCR tests. High-performance metrics were noted, particularly in symptomatic patients within seven days post-symptom onset. The study reaffirms the critical role of rapid testing in pandemic management, positioning ID NOW as a reliable tool for identifying COVID-19 infections.