Cohort 2 enrolled 25 children, randomized to receive 75 mg of once-daily oral zilurgisertib or placebo during a 24-week double-blind period. Twelve received treatment and 13 received placebo. Mean total lesion volume declined by 8.09 cm³ in the treated group, while increasing by 9.14 …
Median investigator-assessed progression-free survival reached 7.2 months in BELLA Part A, and the objective response rate was 59%. For context, Corcept reported median progression-free survival of 5.4 months for Lifyorli plus nab-paclitaxel and 3.9 months for nab-paclitaxel alone in its separate pivotal Phase 3 …
Amy Rock joins as Chief Regulatory and Quality Officer, taking responsibility for global regulatory strategy, quality and pharmacovigilance. Her remit includes engagement with health authorities supporting development of SP001 in IgG4-related disease and potentially other indications.
The European Commission granted orphan designation following a positive opinion from the European Medicines Agency’s Committee for Orphan Medicinal Products. SGT-212 also holds Fast Track, Orphan Drug and Rare Pediatric Disease designations from the U.S. Food and Drug Administration.
The new study is an early feasibility investigation assessing clinical safety and device functionality, including direct Bluetooth communication. Freedom combines implantable sensing technology with an integrated battery and wireless communication capabilities.
Amanat Acquisition Corp (NASDAQ:AMAN), a special purpose acquisition company, and Corxel Pharmaceuticals, Inc. (Corxel US) announced on 26 October 2026 a definitive business combination agreement to create a publicly listed, obesity-focused biopharmaceutical company. The combined company is expected to be listed on the Nasdaq …
Bristol Myers Squibb (NYSE:BMY) and SystImmune announced on 26 October 2026 positive results from a prespecified interim analysis of the Phase 3 PANKU-Lung01 study of izalontamab brengitecan (iza-bren) in previously treated EGFR-mutated non-squamous non-small cell lung cancer (NSCLC). The data were reported by SystImmune's …
Can-Fite BioPharma Ltd. presented final data from its Phase IIa study of namodenoson in advanced pancreatic ductal adenocarcinoma at the European Society for Medical Oncology (ESMO) Congress 2026 in Madrid on 26 October 2026. The Israeli biotechnology company reported that the study achieved its …
HUTCHMED (China) Limited (NASDAQ:HCM) announced on 26 October 2026 positive results from the SANOVO Phase III trial in China, presented at the European Society for Medical Oncology (ESMO) Congress 2026 in Madrid. The trial tested ORPATHYS (savolitinib) plus TAGRISSO (osimertinib) against TAGRISSO alone in …
Actinogen Medical (ASX:ACW) announced on 26 October 2026 that it received a research and development tax incentive (RDTI) rebate of $10,838,793, including interest, from the Australian Tax Office for the 2026 financial year. The payment arrives as the biotechnology company approaches topline results from …