An analysis of stock market movers during the period of this year’s Esmo congress gives biotech watchers little cause for happiness.
The rare disease bile duct cancer is set to be carved up by genetic subtype, and will see two targeted treatments filed soon.
Among small-molecule approaches Europe’s premier oncology conference gives star billing to three Parp inhibitors in ovarian cancer.
Pharming picks up Novartis’s late-stage PI3K inhibitor and plans to launch it for an ultra-rare disease. How will the competition respond?
Orencia’s late-stage failure in Sjögren’s has dashed hopes of a therapy soon, but the mid-stage pipeline is crowded, with Novartis, Glaxosmithkline and Galapagos all…
cMet emerges as the latest genetic mutation that could soon see targeted treatments become available.
The US FDA granted seven approvals in two days last week, including an eagerly awaited thumbs-up for Novartis’s gene therapy Zolgensma.
May looks to be a fairly quiet month for US drug approvals, though Novartis's gene therapy should make headlines.
A patient death notwithstanding, Chi-Med reckons results from the Tatton study justify its US registration strategy.