Universal Health Services Implements Hippocratic AI’s Generative Agents to Enhance Post-Discharge Patient Care

Hippocratic AI, the global leader in safety-focused generative AI agents for healthcare, and Universal Health Services (NYSE: UHS) announced today that GenAI agents that support clinicians by making discharge follow up outreach to patients by phone have been deployed. The…

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Abstractive Health Launches Clinical Time Machine, the First AI Game Built on Real Historical Patient Records

Abstractive Health Launches Clinical Time Machine, the First AI Game Built on Real Historical Patient Records

Abstractive Health has launched Clinical Time Machine, an AI-driven simulation that immerses physicians in diagnostic cases using real historical medical charts. Built on the same HIPAA-compliant platform that powers live summarization of electronic health records (EHRs) in hospital settings, the simulation…

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CORRECTED: 9amHealth Selects Smart Meter for Employer Weight Management Programs with Cellular Scale Integration

CORRECTED: 9amHealth Selects Smart Meter for Employer Weight Management Programs with Cellular Scale Integration

SMART METER SELECTED BY 9AMHEALTH FOR MAJOR EMPLOYER WEIGHT MANAGEMENT PROGRAMS USING CELLULAR WEIGHT SCALE Smart Meter, a pioneer in cellular-enabled weight scale technology, today announced a strategic supply agreement with 9amHealth, a leading provider of comprehensive weight management and…

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4basebio Unveils New Branding to Support Next Phase of Growth in Advanced Genetic Therapies

KalVista Reports FDA Delay on Sebetralstat NDA for Hereditary Angioedema Due to Resource Constraints

KalVista Pharmaceuticals, Inc. (Nasdaq: KALV) today announced that the U.S. Food and Drug Administration (FDA) has notified the Company that it will not meet the PDUFA goal date for the New Drug Application (NDA) for sebetralstat, the Company’s investigational oral…

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Valar Labs’ CHAI Biomarkers Validated in New Study in European Urology for Predicting Outcomes of High Grade Ta Bladder Cancer

Valar Labs’ CHAI Biomarkers Validated in New Study in European Urology for Predicting Outcomes of High Grade Ta Bladder Cancer

Valar Labs, a pioneer in AI-powered diagnostics for oncology, announced the publication of its latest research in European Urology, the highest-impact journal in the field of urology. The peer-reviewed study highlights the performance and clinical impact of Valar Labs’ Vesta platform…

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Cybin Shares Corporate Update and Positive Regulatory Progress for Psychedelic Therapies

Cybin Shares Corporate Update and Positive Regulatory Progress for Psychedelic Therapies

Cybin Inc. (NYSE American:CYBN) (Cboe Canada CA:CYBN) (“Cybin” or the “Company”), a clinical-stage breakthrough neuropsychiatry company committed to revolutionizing mental healthcare by developing new and innovative next-generation treatment options, today provided a corporate update. “It is especially gratifying that at a…

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Astria Therapeutics Shares Promising Early Data from Navenibart Trial in Hereditary Angioedema at EAACI Congress

Astria Therapeutics Shares Promising Early Data from Navenibart Trial in Hereditary Angioedema at EAACI Congress

 a biopharmaceutical company focused on developing life-changing therapies for allergic and immunologic diseases, today announced positive initial results from the target enrollment group in the ongoing ALPHA-SOLAR long-term open-label trial evaluating navenibart (STAR-0215), a monoclonal antibody inhibitor of plasma kallikrein,…

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Zai Lab Unveils Preclinical Data on ZL-1503 for Atopic Dermatitis at EAACI 2025

Zai Lab Unveils Preclinical Data on ZL-1503 for Atopic Dermatitis at EAACI 2025

Zai Lab Limited (NASDAQ: ZLAB; HKEX: 9688) announced new data from its preclinical study of ZL-1503, the Company’s promising IL-13/IL-31R bispecific antibody, demonstrating its ability to simultaneously suppress the inflammatory and pruritogenic (itch-causing) pathways in atopic dermatitis (AD). The findings,…

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FDA Approves KEYTRUDA® for PD-L1+ Head & Neck Cancer in Neoadjuvant and Adjuvant Settings

FDA Approves KEYTRUDA® for PD-L1+ Head & Neck Cancer in Neoadjuvant and Adjuvant Settings

FDA Approves KEYTRUDA® for PD-L1+ Head & Neck Cancer in Neoadjuvant and Adjuvant Settings Merck (NYSE: MRK), known as MSD outside of the United States and Canada, announced that the U.S. Food and Drug Administration (FDA) has approved KEYTRUDA® (pembrolizumab), Merck’s…

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