Boehringer beats Bayer to the regulators
The FDA will rule on a low dose of zongertinib in the summer.
The FDA will rule on a low dose of zongertinib in the summer.
While Cogent joins the FGFR party.
But could toxicity be holding back filing plans?
The group will present the first clinical data on its KRAS G12D-selective project RMC-9805.
Spectrum’s poziotinib failed in HER2 exon 20 lung cancer, but that isn’t stopping Boehringer and Bayer.
A year-end pipeline update reveals Boehringer Ingelheim’s oncology priorities.
Projects from the likes of BioNTech, Transgene and Scancell will feature, but still have much to prove.