Success for Alecensa as it meets primary endpoint in another patient group
Genentech will meet with the FDA and EMA after the successful Phase III study of Alecensa in early-stage ALK-positive NSCLC.
01 September 2023
01 September 2023
Genentech will meet with the FDA and EMA after the successful Phase III study of Alecensa in early-stage ALK-positive NSCLC.
Bayer adds three new Phase III studies to the Kerendia clinical development programme.
Novo Nordisk's obesity drugs are driving Danish growth as well as record profits as the company becomes second-most valuable in Europe.
Alkermes settled the lawsuit with Teva, allowing the latter to market the generic version of Vivitrol from January 2027.
No serious adverse events or significant changes in plasma amino acid levels were observed in the study.
In the Phase I monotherapy study, AML patients treated with FHD-286 showed recoveries in absolute neutrophil count.
The study is being conducted in partnership with researchers from the gastroenterology and hepatology department at Erasmus MC.
The trial will measure LAM-001's tolerability, safety and activity in WHO-functional Class III adults with advanced PAH.
Enter the Excellence Awards today! This program offers multiple benefits, such as gaining visibility among the market, your employees, and prospective clients for your achievement. To learn more about benefits, entry details, and available marketing packages, download the Research Guide.
There are currently 13 authorized/approved COVID-19 vaccines in the 7 major pharma markets. Currently, vaccine developers plan to launch updated boosters prior to the upcoming 2023 fall season to target the latest dominant strain, Omicron XBB.1.5. Per GlobalData analysis, mRNA vaccines will likely continue to dominate the market, though as the pandemic winds down, the global COVID-19 vaccines market is expected to decline.
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