Abridge Secures $250M Series D, Unveils New Contextual Reasoning Engine for Healthcare Abridge, a leader in generative AI for clinical conversations, has secured a $250 million Series D funding round. This milestone comes as the company surpasses 100 deployments across…
FDA Approves GSK’s PENMENVY 5-in-1 Meningococcal Vaccine GSK plc (LSE/NYSE: GSK) has announced that the U.S. Food and Drug Administration (FDA) has approved its PENMENVY vaccine (Meningococcal Groups A, B, C, W, and Y Vaccine) for use in individuals aged…
LimmaTech Begins Phase 1 Trial of Staphylococcus aureus Vaccine LBT-SA7 LimmaTech Biologics AG, a clinical-stage biotech company focused on developing vaccines for life-threatening diseases, announced the vaccination of the first participants in a Phase 1 controlled study of its multivalent…
UK’s EDX Medical Develops New ‘Super Test’ for Prostate Cancer Scientists in Cambridge have created a groundbreaking new ‘super test’ for prostate cancer, aiming to transform the way the disease is screened and diagnosed. This innovative test is designed to…
Innate Pharma’s Lacutamab Receives FDA Breakthrough Therapy Designation for Sézary Syndrome Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA) has announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation (BTD) to lacutamab, an innovative anti-KIR3DL2…
Two Dedicated Team Members Awarded the Graeme Rabbits Scholarship Two deserving individuals are one step closer to achieving their career aspirations in behavioural neuroscience and social work, thanks to receiving $10,000 each toward their tertiary education. The Graeme Rabbits Scholarship,…
Five-Year Sotyktu (Deucravacitinib) Data Show Consistent Safety and Durable Response in Psoriasis Bristol Myers Squibb (NYSE:BMY) has announced new five-year data from the POETYK PSO long-term extension (LTE) trial, evaluating Sotyktu (deucravacitinib) in adult patients with moderate-to-severe plaque psoriasis. The…
Samsung Bioepis Gains EC Approval for Denosumab Biosimilar (OBODENCE™, XBRYK™) Samsung Bioepis Co., Ltd. has announced that the European Commission (EC) has granted marketing authorization for two denosumab biosimilars, OBODENCE™ (60 mg prefilled syringe) and XBRYK™ (120 mg vial), which…
MED-EL USA Gets FDA Approval for SONNET 3 Audio Processor MED-EL USA has announced the U.S. Food and Drug Administration (FDA) approval of its latest innovation, the SONNET 3 audio processor, designed for use with MED-EL cochlear implants. As the…
FDA Grants Full Approval to Deciphera’s ROMVIMZA™ (vimseltinib) for Symptomatic TGCT Ono Pharmaceutical Co., Ltd. has announced that the U.S. Food and Drug Administration (FDA) has granted full approval for ROMVIMZA™ (vimseltinib), a kinase inhibitor, for the treatment of adult…
UroGen Shares ENVISION Trial Subgroup Analysis on Tumor Burden and UGN-102 Response UroGen Pharma Ltd. (Nasdaq: URGN) announced results from subgroup analyses of the pivotal ENVISION study, assessing the impact of tumor burden and focality on the response to UGN-102,…
IMFINZI® Regimen Boosts Survival in Muscle-Invasive Bladder Cancer: NIAGARA Phase III Post-Hoc Analysis A post-hoc exploratory analysis from the Phase III NIAGARA trial has shown that AstraZeneca’s IMFINZI® (durvalumab), when administered perioperatively with neoadjuvant chemotherapy, significantly improves event-free survival (EFS)…