
Celgene’s Abraxane, in combination gemcitabine, has failed to meet its primary endpoint in a pivotal Phase 3 trial of patients …

A new class of cholesterol lowering drugs may help patients who are unable to take statins, according to a study …

Richard Francis is set to step down his role as Chief Executive of Novartis’ generics arm Sandoz after five years’ …

A California jury has ordered American healthcare conglomerate Johnson & Johnson to pay more than $29 million to a woman …

Following the surprise resignation of current FDA Commissioner Dr Scott Gottlieb a week earlier, Dr Norman ‘Ned’ Sharpless, Director of …

Janssen’s ulcerative colitis treatment, Stelara (ustekinumab subcutaneous) has shown positive results as maintenance therapy in phase 3 trials. The study …

Eli Lilly’s vascular endothelial growth factor (VEGF) Receptor 2 antagonist Cyramza (ramucirumab) has succeeded in hitting its primary endpoint at …

The healthcare industry could take up to five years to stabilise in the event of a no-deal Brexit, according to …

The FDA has approved a new generic version of blood pressure drug valsartan. The approval comes amid shortages in supply …

French company Innate Pharma have announced the appointment of Jennifer Butler to the position of Executive Vice President and General …

Partners Sanofi and Regeneron have both revealed that their jointly developed drug Dupixent (dupilumab) has been authorised by the FDA …

Indian firm Dr Reddy’s is seeking at least $70 million from British firm Indivior Plc as compensation for lost sales …

Britain’s cost effectiveness body NICE have recommended Janssen Pharmaceutical’s Darzalex in combination with Velcade and dexamethasone (DVd), for use within …

Patients in the US will now be able to access another biosimilar version of Herceptin (trastuzumab) with the FDA approval …

Scotland’s cost effectiveness body has refused to fund Novartis’ CAR T therapy Kymriah for adult patients with lymphoma. The Scottish …

Louis Goss asks what the future might hold for the safety of pharmaceuticals and looks into why crucial pharmacovigilance practices …

Roche’s Ventana PD-L1 Assay has become the first FDA-approved companion diagnostic for the identification of patients with triple-negative breast cancer …

AMAG Pharmaceuticals’ Makena (hydroxyprogesterone caproate) has failed to meet its co-primary endpoints in a trial of patients with a history …

Dengvaxia, Sanofi’s vaccine for dengue fever, has been burdened with further negative scrutiny after the FDA’s vaccine advisory panel passed …

The US Department of Justice has launched an investigation into the sales and marketing practices of San Diego firm Acadia …