7,114 press releases indexed under healthcare.
Elizabeth Tucker and Brett Travers join the firm's health care regulatory and real estate practices, signaling rapid investment in the Missouri market. ST. LOUIS, Sept. 3, 2026 /PRNewswire/ -- Hall Render, the nation's leading law firm focused exclusively on health care, is pleased to...
San Diego, California--(Newsfile Corp. - September 3, 2026) - Shareholder rights law firm Robbins LLP informs investors that a class action was filed on behalf of all persons and entities who purchased or otherwise acquired Fractyl Health, Inc. (NASDAQ: GUTS) securities between January 13, 2025 and January 29, 2026 (the "Class Period"). Fractyl is a metabolic therapeutics company that develops therapies for the treatment of type 2 diabetes ("T2D") and obesity.The complaint alleges that Fractyl...
HONG KONG, Sept 3, 2026 - (ACN Newswire) - Everest Medicines today announced that China’s National Medical Products Administration (NMPA) has approved CARDAMYST(R) (etripamil) for the conversion of acute symptomatic episodes of paroxysmal supraventricular tachycardia (PSVT) to sinus rhythm in adults. As Everest's first innovative therapy approved in the cardiovascular field, CARDAMYST further expands the Company‘s cardiovascular portfolio. The approval marks another important milestone in the execution of Everest's commercialization strategy and reinforces the Company's capability to bring innovative therapies to patients in China. CARDAMYST (etripamil) nasal spray is a novel, rapid-acting calcium channel blocker administered as needed via a convenient, portable nasal spray. It offers rapid onset of action, favorable tolerability, and the potential for at-home self-administration, enhancing patient accessibility. CARDAMYST is currently the only self-administered treatment for adults with PSVT to rapidly treat episodes. Treatment effects observed as early as five minutes after administration, with nearly two-thirds of patients achieving conversion to sinus rhythm within 30 minutes, reducing the need for emergency medical interventions and filling a critical gap in out-of-hospital, self-administered treatment options for acute symptomatic episodes of PSVT in China. PSVT is a type of tachyarrhythmia characterized by the sudden onset and termination of episodes of rapid, regular heart rhythm. Approximately 2.3 to 4 per 1,000 individuals are affected by PSVT, representing an estimated 3 to 6 million patients in China. During episodes, the heart rate spike is unpredictable and may last several hours. The rapid heart rate often causes disabling severe palpitations, shortness of breath, chest discomfort, dizziness or lightheadedness, and distress, forcing patients to limit their daily activities. The management of acute PSVT episodes in China has long relied primarily on hospital-based emergency care, highlighting the need for an on-demand treatment option that patients can self-administer outside of healthcare settings. “The approval of CARDAMYST addresses a critical unmet need by introducing the first innovative therapy that enables patients to self-administer treatment for acute PSVT episodes in China,” said Professor Changsheng Ma, M.D., Principal Investigator of the Phase III JX02002 study, Director of Cardiology Department at Beijing Anzhen Hospital, and President of the Chinese Society of Cardiology, Chinese Medical Association, “Both the global pivotal Phase III RAPID trial and the China Phase III JX02002 study demonstrated its rapid onset, robust efficacy, and favorable safety profile. We believe this innovative therapy has the potential to transform the treatment paradigm for acute PSVT episodes by enabling timely, patient-initiated treatment, reducing the need for emergency medical intervention, and ultimately improving patients' quality of life.” “The approval of CARDAMYST marks an important milestone, introducing the first out-of-hospital, patient-administered treatment option for acute PSVT episodes in China,” said Mr. Rogers Yongqing Luo, Chief Executive Officer of Everest Medicines. “As the only innovative therapy currently available that enables patients to self-administer treatment for PSVT episodes outside of healthcare settings, CARDAMYST offers a new on-demand treatment option. With treatment effects observed as early as five minutes after administration, CARDAMYST enables patients to manage episodes outside of a healthcare setting, giving them greater control over their condition and potentially reshaping the treatment paradigm for PSVT in China. Leveraging our proven commercialization capabilities, we look forward to accelerating the launch of CARDAMYST in China to address the significant unmet needs of patients with PSVT and realize its long-term clinical and societal value." The approval of CARDAMYST was supported by the global pivotal Phase III RAPID trial and the Phase III JX02002 study in China. Both studies met their primary endpoints. The RAPID trial achieved its primary endpoint with 64% of participants who self-administered etripamil (N=99) converting from supraventricular tachycardia (SVT) to sinus rhythm within 30 minutes compared to 31% on placebo (N=85) (HR = 2.62; p<0.001). The study results were published in The Lancet in 2023. In the JX02002 study, among participants with PSVT episodes (N=84), a greater number of patients receiving etripamil achieved conversion to sinus rhythm within 30 minutes, compared with placebo (N=84) (hazard ratio [HR] = 3.002; p=0.0005). In December 2025, CARDAMYST was approved by the U.S. Food and Drug Administration (FDA), becoming the first and only self-administered nasal spray in more than 30 years capable of converting paroxysmal supraventricular tachycardia (PSVT) to sinus rhythm in adults. CARDAMYST is also in Phase III clinical development for atrial fibrillation with rapid ventricular response (AFib-RVR), with positive Phase II results supporting its advancement. CARDAMYST has the potential to benefit more than 12 million patients in China, including those with PSVT and AFib-RVR. The approval of CARDAMYST(R) further strengthens Everest Medicines’ presence across the cardiovascular, kidney, and metabolic (CKM) disease areas and broadens its innovative product portfolio. As the Company’s first innovative drug approved in the cardiovascular disease field, CARDAMYST(R) also complements the Company’s existing portfolio and creates opportunities for portfolio synergies. Leveraging its established commercialization capabilities, Everest Medicines will move forward with the launch of CARDAMYST(R) in China while advancing its development in additional cardiovascular indications, including AFib-RVR, to bring new treatment options to more patients with cardiovascular disease. Copyright 2026 ACN Newswire. All rights reserved. www.acnnewswire.com
(PR-inside.com) €4 million European-funded DIGICAP project brings together 19 organizations to replace document-based conformity assessments with machine-readable data. DistillerSR named one of five technology providers building the framework. OTTAWA, ON / ACCESS Newswire / September 3, 2026 / DistillerSR , the market leader in AI-enabled literature review automation and evidence management, today announced its participation in DIGICAP (DIGItalisation of the Conformity Assessment Process), a €4 million European initiative uniting 19 organizations across 12 EU countries to digitalize how medical devices and in vitro diagnostics are certified for the European market. The project is funded under Horizon Europe, the world's largest multinational research ..
€4 million European-funded DIGICAP project brings together 19 organizations to replace document-based conformity assessments with machine-readable data. DistillerSR named one of five technology providers building the framework.
TrialBase Litigation Intelligence ( ai.trialbase.com ) now delivers trial plans, jury selection strategy, venue-specific voir dire guidance, opening statements, and witness testimony preparation within a single litigation platform. These features build upon TrialBase's existing support for case evaluation, discovery, deposition preparation, medical chronologies, demand letters, and litigation strategy. - - Unlike point solutions that focus on isolated tasks, TrialBase provides a unified p... Read the full story at https://www.webwire.com/ViewPressRel.asp?aId=359915
CHICAGO, Sept. 3, 2026 /PRNewswire/ -- The National Center for Children's Vision and Eye Health at Prevent Blindness (NCCVEH) has named Mike DeWine, Governor of Ohio, the recipient of the 12th annual Bonnie Strickland Champion for Children's Vision Award, for the "Ohio Student Eye Exam...
NAPERVILLE, Ill., Sept. 3, 2026 /PRNewswire/ -- Specialty physicians looking for more support and resources have increasingly faced a familiar choice: sell to private equity or join a larger health system. One Health Partners has created another option. Today, One Health Partners unveiled...
Cincinnati-based breast care company expands capacity and provider support to help minimize diagnostic delays and restore patient access to critical procedures CINCINNATI, Sept. 3, 2026 /PRNewswire/ -- Mammotome, a Danaher Company and global leader in breast care innovation, has expanded...
The FDA-cleared upper-arm monitor is clinically validated for pregnancy and adults with diabetes, pairing a large display and voice guidance with connected records for home use.
Integrated seamlessly with Curve, Curve Memberships helps practices identify enrollment opportunities, automate patient outreach and keep payments connected to billing and collections ALPHARETTA, Ga., Sept. 3, 2026 /PRNewswire/ -- Curve Dental®, the leader in AI-powered, cloud-native,...
As food insecurity and living costs rise, the partnership delivers direct support and connects vulnerable families to resources that promote long-term health and well-being. NEW YORK, Sept. 3, 2026 /PRNewswire/ -- Public Health Solutions (PHS), in partnership with ModifyHealth, held a...