The U.S. Food and Drug Administration on Friday approved Incyte Corp’s treatment for acute Graft versus Host disease (GvHD), an inflammatory response by the immune system after a bone marrow transplant.

The U.S. Food and Drug Administration (FDA) said on Friday it approved Novartis AG’s treatment in combination with hormone therapy fulvestrant for postmenopausal women, as well as men, with a form of advanced...

De Committee for Medicinal Products for Human Use (CHMP) heeft een positief advies gegeven over nieuwe handelsvergunningen voor acht geneesmiddelen.

The Food and Drug Administration (FDA) has accepted for Priority Review the supplemental New Drug Application (sNDA) for Invokana (canagliflozin; Janssen) to reduce the risk of end-stage renal disease (ESRD) and renal...

Nederlanders geven het vertrouwen in hun eigen medicijnen een 7,9. Bijna de helft geeft aan dat het soms moeten wisselen redelijk tot veel invloed heeft op dat vertrouwen. Dat blijkt uit onderzoek van het Nivel, in...

European Medicines Agency’s (EMA) Pharmacovigilance Risk Assessment Committee (PRAC) has recommended that the marketing authorisations for fenspiride medicines be revoked, so the medicines can no longer be...

Roche announced that the US Food and Drug Administration (FDA) has approved Venclexta (venetoclax) in combination with Gazyva (obinutuzumab) for the treatment of people with previously untreated chronic lymphocytic...

The old adage “better late than never” may be overused, but for Celgene, it certainly applies to England’s cost watchdogs and their stance toward the company’s multiple myeloma flagship drug Revlimid.

The US Food and Drug Administration (FDA) approved Fragmin (dalteparin sodium) injection, for subcutaneous use, to reduce the recurrence of symptomatic venous thromboembolism (VTE) in paediatric