Eisai’s Leqembi deemed too costly for NHS
Though the UK became the first country in Europe to authorize use of Eisai and Biogen’s early Alzheimer’s disease drug,…
Though the UK became the first country in Europe to authorize use of Eisai and Biogen’s early Alzheimer’s disease drug,…
Pfizer and BioNTech have announced that a Phase III trial studying their investigational combination mRNA vaccine for the treatment of…
Pfizer has announced positive topline results from a pivotal late-stage study of its respiratory syncytial virus (RSV) vaccine, Abrysvo, in…
In a bid to further diversify its pipeline, Merck & Co (MSD) has announced that it is set to acquire…
Eisai has announced that patients undergoing continuous treatment with its anti-amyloid therapy Leqembi (lecanemab) for three years have shown a…
As the industry paints an increasingly clearer picture for Alzheimer’s disease pathologies, treatments are becoming more inclusive of non-pharmacological lifestyle…
Mesoblast has announced that the US Food and Drug Administration (FDA) has accepted a resubmitted biologics license application (BLA) for…
Bristol Myers Squibb has announced that the European Medicines Agency (EMA) will begin a review of its application covering the…
Atara Biotherapeutics has announced that the US Food and Drug Administration (FDA) has awarded a priority review for its biologics…
Delix Therapeutics is planning to initiate two studies to evaluate patients with major depression investigating its lead neuroplastogen candidate, DLX-001,…