Press Releases

Company press releases and official corporate announcements.

A centralized feed of corporate press releases, earnings announcements, mergers, and official statements. Content is presented for informational purposes and may require additional analysis for market relevance.

Articles

23,663 total articles

ODDITY Tech Reports Second Quarter 2026 Results, Expects Sequential Revenue Improvement in the Third Quarter

ODDITY Tech Reports Second Quarter 2026 Results, Expects Sequential Revenue Improvement in the Third Quarter

ODDITY Tech Ltd. reported Q2 2026 net revenue of $181 million, down 25% year-over-year, with adjusted EBITDA of $13 million and net income of $13 million. The company highlighted strong revenue growth in its SpoiledChild brand and promising early results from METHODIQ. It is addressing a technical advertising issue with its largest partner affectin…

Autolus Therapeutics Announces FDA RMAT Designation Granted to Obe-cel for the Treatment of Systemic Lupus Erythematosus and Lupus Nephritis

Autolus Therapeutics Announces FDA RMAT Designation Granted to Obe-cel for the Treatment of Systemic Lupus Erythematosus and Lupus Nephritis

Autolus Therapeutics announced that the FDA granted RMAT designation to its T cell therapy candidate obecabtagene autoleucel (obe-cel) for treating systemic lupus erythematosus (SLE) and lupus nephritis (LN), accelerating development and regulatory review. The company plans further clinical data presentations and continues enrollment in a pivotal P…

Pyxis Oncology Announces Positive Updated Data from Phase 1 Monotherapy Study of Micvotabart Pelidotin (MICVO) in Second-Line and Beyond Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma (2L+ R/M HNSCC)

Pyxis Oncology Announces Positive Updated Data from Phase 1 Monotherapy Study of Micvotabart Pelidotin (MICVO) in Second-Line and Beyond Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma (2L+ R/M HNSCC)

Pyxis Oncology reported positive updated results from its Phase 1 monotherapy study of micvotabart pelidotin (MICVO) in second-line and beyond recurrent/metastatic head and neck squamous cell carcinoma (2L+ R/M HNSCC). The study showed a 36% confirmed objective response rate, 94% disease control rate, median progression-free survival of 6.2 months,…

Rezolute Provides Update on FDA Review of its Phase 3 sunRIZE Study Results in Congenital Hyperinsulinism

Rezolute Provides Update on FDA Review of its Phase 3 sunRIZE Study Results in Congenital Hyperinsulinism

Rezolute announced that the FDA review of their Phase 3 sunRIZE study data for their drug ersodetug in treating congenital hyperinsulinism (HI) is ongoing without a defined timeline. While the study did not meet its primary endpoint for statistical significance, secondary analyses indicate glycemic improvements. The open-label extension phase conti…

Kura Oncology Launches Caspian Therapeutics with $50 Million Financing to Advance Menin Inhibition as a Potential Disease-Modifying Approach for Diabetes

Kura Oncology Launches Caspian Therapeutics with $50 Million Financing to Advance Menin Inhibition as a Potential Disease-Modifying Approach for Diabetes

Kura Oncology has established Caspian Therapeutics, a separately financed subsidiary focused on advancing KO-7246, a next-generation menin inhibitor designed for diabetes and cardiometabolic diseases. Caspian raised $50 million led by BVF Partners and supported by key biotech investors including Eli Lilly. Preclinical studies show promising results…

Satellos Announces Forazapadin as Assigned International Nonproprietary Name for Lead Drug Candidate, SAT-3247

Satellos Announces Forazapadin as Assigned International Nonproprietary Name for Lead Drug Candidate, SAT-3247

Satellos Bioscience announced that their lead oral small molecule drug candidate, previously known as SAT-3247, has been assigned the International Nonproprietary Name (INN) 'forazapadin.' The drug targets AAK1 to promote muscle regeneration and is currently in Phase 2 clinical trials for Duchenne muscular dystrophy (DMD), with plans to initiate a …

INLIF LIMITED Announces Adjournment of Extraordinary General Meeting

INLIF LIMITED Announces Adjournment of Extraordinary General Meeting

INLIF LIMITED announced that its Extraordinary General Meeting of Shareholders originally scheduled for September 8, 2026, was adjourned due to insufficient shareholder attendance to meet quorum requirements. The meeting is set to reconvene on September 15, 2026. Previously submitted votes remain valid, and shareholders who have not yet voted are e…

Eledon Pharmaceuticals Announces Presentation at the International Congress of The Transplantation Society

Eledon Pharmaceuticals Announces Presentation at the International Congress of The Transplantation Society

Eledon Pharmaceuticals announced an upcoming oral presentation at the International Congress of The Transplantation Society showcasing long-term safety and efficacy data of its lead investigational drug, tegoprubart, for preventing kidney transplant rejection. The data come from the Phase 2 BESTOW trial and its extension, highlighting the drug's po…

Cocrystal Pharma Announces Last Subject Dosed in Phase 1b Human Challenge Study Evaluating CDI-988 for Norovirus Prevention and Treatment

Cocrystal Pharma Announces Last Subject Dosed in Phase 1b Human Challenge Study Evaluating CDI-988 for Norovirus Prevention and Treatment

Cocrystal Pharma announced that the last subject has been dosed in its Phase 1b norovirus challenge study evaluating CDI-988 as a preventive and treatment for norovirus infections. This study is the first clinical trial of a direct-acting antiviral specifically targeting norovirus, aiming to address a significant unmet medical need. CDI-988 has sho…

Can-Fite: Publication Reports Improvement in Decompensated Cirrhosis with Namodenoson and Successful Bridging to Liver Transplantation

Can-Fite: Publication Reports Improvement in Decompensated Cirrhosis with Namodenoson and Successful Bridging to Liver Transplantation

Can-Fite BioPharma announced publication of a peer-reviewed case report detailing the successful treatment of a patient with advanced decompensated liver cirrhosis using their drug Namodenoson, resulting in resolution of ascites and regression of esophageal varices. The patient remained clinically stable for 28 months on treatment before undergoing…

Telix to Present at the Morgan Stanley 24th Annual Global Healthcare Conference and H.C. Wainwright 28th Annual Global Investment Conference

Telix to Present at the Morgan Stanley 24th Annual Global Healthcare Conference and H.C. Wainwright 28th Annual Global Investment Conference

Telix Pharmaceuticals Limited announced that its senior executives will present at the Morgan Stanley 24th Annual Global Healthcare Conference and the H.C. Wainwright 28th Annual Global Investment Conference. The company, a global radiopharmaceutical leader in cancer theranostics, aims to showcase its commercial progress and future plans to investo…

Einride Expands Defense Offering With Mission Planning and Operational Decision-Making for Autonomous Logistics

Einride Expands Defense Offering With Mission Planning and Operational Decision-Making for Autonomous Logistics

Einride AB announced a strategic partnership with UNIQAI Systems to enhance its autonomous logistics platform with AI-driven mission planning and operational decision-making capabilities tailored for defense and national security clients. Building on its existing autonomous freight technology and previous collaborations, Einride aims to address a s…

MannKind and Rose Pharma Inc Enter Licensing and Collaboration Agreement to Develop an Inhaled Rapid-Acting, Short-Duration GLP-1 for Weight Management

MannKind and Rose Pharma Inc Enter Licensing and Collaboration Agreement to Develop an Inhaled Rapid-Acting, Short-Duration GLP-1 for Weight Management

MannKind Corporation has entered into a licensing and collaboration agreement with Rose Pharma Inc. to develop ROSE-010 Technosphere, a rapid-acting, short-duration inhaled GLP-1 receptor agonist for weight management. MannKind will provide pharmaceutical development and manufacturing support through Phase 1b trials, receive equity in Rose Pharma, …

Sysco Reaffirming Fiscal 2027 Guidance; Introducing $500 Million Multi-Year AI Powered Efficiency Program; Raising Mid-Term Financial Algorithm Targets

Sysco Reaffirming Fiscal 2027 Guidance; Introducing $500 Million Multi-Year AI Powered Efficiency Program; Raising Mid-Term Financial Algorithm Targets

Sysco Corporation reaffirmed its fiscal 2027 financial guidance with expected adjusted EPS growth of 9%-11% and announced a new $500 million multiyear AI-powered efficiency program aimed to reduce structural costs by fiscal 2029. The company also raised its mid-term financial targets for net sales and adjusted EPS growth for fiscal years 2028 and 2…

RadNet to Host Free Prostate Cancer Webinar on September 19, 2026

RadNet to Host Free Prostate Cancer Webinar on September 19, 2026

RadNet, Inc., a leading US outpatient imaging services provider, announced a free webinar on September 19, 2026, focused on prostate cancer risk, screening, diagnosis, and treatment advancements, including the use of prostate MRI and AI. The event aims to educate men and families during Prostate Cancer Awareness Month by featuring expert panelists …

Radware H1 2026 Global Threat Report Shows Web DDoS Attacks Jump More Than 110% as Cyber Threats Accelerate

Radware H1 2026 Global Threat Report Shows Web DDoS Attacks Jump More Than 110% as Cyber Threats Accelerate

Radware Ltd. (NASDAQ: RDWR) released its H1 2026 Global Threat Analysis Report revealing a sharp increase in cyberattack activities, including a 110.6% rise in Web DDoS attacks and a doubling of malicious web application and API attacks compared to 2025. The report emphasizes rapid exploitation of vulnerabilities, accelerated by AI technologies, an…

RadNet, Inc. to Present at the Morgan Stanley 24th Annual Global Healthcare Conference on Wednesday, September 16th, 2026

RadNet, Inc. to Present at the Morgan Stanley 24th Annual Global Healthcare Conference on Wednesday, September 16th, 2026

RadNet, Inc., a leading US provider of diagnostic imaging services and related technology solutions, announced that its Executive Vice President and CFO, Mark Stolper, will present at the Morgan Stanley 24th Annual Global Healthcare Conference. The company operates a large network of outpatient imaging centers across multiple US states and offers A…

Kilbourne Graphite Project Advances Through Key Permitting Milestones

Kilbourne Graphite Project Advances Through Key Permitting Milestones

Titan Mining Corporation announced substantial advancements in federal and state permitting processes for its Kilbourne Graphite Project in New York as it remains on track for commercial natural flake graphite production by 2028. The project has received significant federal support, including financing interest from the U.S. Export-Import Bank, and…

Oral Infigratinib Shows Meaningful Benefits Beyond Growth Within 52 Weeks in Children with Achondroplasia in the Phase 3 PROPEL 3 Trial

Oral Infigratinib Shows Meaningful Benefits Beyond Growth Within 52 Weeks in Children with Achondroplasia in the Phase 3 PROPEL 3 Trial

BridgeBio Pharma announced positive results from their Phase 3 PROPEL 3 trial of oral infigratinib in children with achondroplasia, demonstrating benefits beyond increased growth including stabilization of sleep apnea, reduced ear infections, and improved body composition. The drug maintained sustained growth improvements and safety over three year…

Premium Catering (Holdings) Limited Receives NASDAQ Notice Related to Late Filing of Its Interim Report

Premium Catering (Holdings) Limited Receives NASDAQ Notice Related to Late Filing of Its Interim Report

Premium Catering (Holdings) Limited announced it received a NASDAQ notice for not timely filing its interim report for the half year ended December 31, 2025, resulting in non-compliance with NASDAQ listing rules. The company has 60 days to submit a compliance plan and potentially up to 180 days to regain compliance, failing which it risks delisting…