AbbVie is eyeing regulatory filings in 2027 for the skin disease drug lutikizumab after clearing multiple endpoints in a late-stage trial, but the results have disappointed...
NORTH CHICAGO, Ill., Oct. 22, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced positive topline results from the Phase 3 INTREPID study evaluating the safety and...
A Moderna and Merck personalized mRNA cancer vaccine reduced the risk of disease recurrence in patients with melanoma by 42% compared to standard treatment.
AbbVie's lutikizumab, an experimental therapy for a chronic skin condition, succeeded in a late-stage trial but missed market expectations.
As displayed in the Federal Register notice on August 1, 2018, FDA is conducting a Complex Innovative Designs (CID) Meeting Program to support the goal of...
A small, uncontrolled phase II trial associated eight weeks of oxaloacetate with improved cognition, fatigue and physical functioning in 16 breast cancer survivors who completed treatment.
Brepocitinib is on a roll. After winning approval for an autoimmune skin disease, Roivant Sciences subsidiary Priovant’s drug hit all primary and secondary endpoints in a...
Reforms to the regulatory framework for clinical research in the UK are starting to deliver, with delivery times down 35%, according to new data.
A retrospective cohort of 2,278 chemotherapy-treated gastrointestinal cancer patients found that 88.1% visited an emergency department and 86.5% were admitted to a hospital during their first...
A randomized block-design field experiment found that co-inoculating mungbean with Bradyrhizobium and selected PGPR improved yield, grain protein and rhizosphere biological measures under the tested conditions.
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