A new dawn for tovorafenib
The FDA's tough stance notwithstanding, Ojemda gets an accelerated green light.
The FDA's tough stance notwithstanding, Ojemda gets an accelerated green light.
A roundup of the first quarter's key oncology drug approvals and rejections.
The drug adds a new use to its US label, but Takeda’s 2017 Ariad acquisition still looks expensive.
Early activity of JANX007 in prostate cancer sees Janux stock gain 190%.
A look at big oncology deals since 2016 suggests that there have been more duds than successes.
The end of three licensed assets sees Takeda take a step back from autologous cell therapy.
Rusfertide’s big readout will now not come until 2025.