Articles

  • 1 week ago | hcplive.com | Abigail Brooks

    The American Thoracic Society’s (ATS) International Conference took place in San Francisco, California, from May 18-21, 2025. Coined as the home of pulmonary, critical care, and sleep professionals, the 4-day conference featured the latest advances in each of these spaces, including updates on key topics in asthma, chronic obstructive pulmonary disease (COPD), lung cancer, sepsis, acute respiratory distress, sleep apnea, and more.

  • 1 week ago | hcplive.com | Abigail Brooks

    The US Food and Drug Administration (FDA) has accepted and granted priority review to Otsuka Pharmaceutical Development & Commercialization’s Biologics License Application (BLA) for sibeprenlimab for the treatment of IgA nephropathy (IgAN).1Announced on May 27, 2025, the BLA acceptance is supported by data from the phase 3 VISIONARY trial, which met its primary endpoint at the prespecified interim analysis, as well as results from the Phase 2 ENVISION clinical trial.

  • 2 weeks ago | businessandamerica.com | Abigail Brooks

    This week, Julie Eshelman has been holding her breath, waiting to see if President Donald Trump delivers on his campaign promise to make in vitro fertilization free. Eshelman is a military wife and, thanks to IVF, a mom. She first began fertility treatments in 2016, and she and her husband finally welcomed a baby girl — five years, several miscarriages and $80,000 later.

  • 2 weeks ago | hcplive.com | Abigail Brooks

    New research is shedding light on dupilumab’s sustained impact on lung function parameters in patients with chronic obstructive pulmonary disease (COPD) and type 2 inflammation.1 Pooled data from the phase 3 BOREAS and NOTUS trials were presented at the American Thoracic Society (ATS) International Conference 2025 by Meilan Han, MD, MS, a professor of medicine and chief of the division of pulmonary and critical care at the University of Michigan Health.1 A fully human monoclonal antibody,...

  • 2 weeks ago | hcplive.com | Abigail Brooks

    Hydronidone met the primary endpoint in a pivotal phase 3 trial evaluating its efficacy and safety for the treatment of liver fibrosis in patients with chronic hepatitis B (CHB) in China, according to a press release from Gyre Therapeutics.1Announced on May 22, 2025, the trial met its primary endpoint for ≥1-stage regression in liver fibrosis compared to placebo.

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