
AstraZeneca has unveiled positive new Phase 3 data for the combination of Imfinzi (durvalumab) and anti-CTLA4 antibody tremelimumab with chemotherapy …

Patient insights are crucial. As you already know, they are the key to the creation of successful, targeted programmes and …

Gilead’s impending regulatory submission of its JAK inhibitor filgotinib to the FDA for the treatment of rheumatoid arthritis has been …

The Biotechnology and Biological Sciences Research Council (BBSRC) and UK Research and Innovation (UKRI) have awarded a funding injection of …

New research from GlobalData has forecast that the worldwide market for ovarian cancer is set to expand at a compound …

Nigeria has seen almost 400 of its medicine dispensaries shut down over “unethical practices and lack of compliance, it has …

Astellas has revealed that the European Commission has awarded marketing approval for Xospata (gilteritinib) as an oral, once-daily monotherapy for …

Seattle Genetics, a strong competitor in the breast cancer space, has reported topline results in its phase 3 study evaluating …

It’s another end of the week here at Pharmafile and here we run down our top 10 articles and features …

BioSciences in the UK has received a massive boost of £18.5 million awarded from the Biotechnology and Biological Sciences Research …

Biogen is planning to seek approval for its experimental drug aducanumab, that could potentially be first to treat Alzheimer’s and …

For its fifth annual Europe conference, FlyPharma chose Copenhagen as its host city to address the latest supply chain challenges …

Novartis has signed a collaboration and license agreement with Pliant Therapeutics to develop and commercialise preclinical asset PLN-1474 which is …

The Irish biopharma company expects to complete most of the job cuts by end of this year and will take …

Novartis has announced that the European Commission has approved a label update for the up-titration of Cosentyx (secukunumab) to 300mg …

A new report has warned that poorly implemented electronic medication systems in the NHS could potentially lead to fatal medication …

The US FDA has approved GlaxoSmithKline’s Zejula (niraparib) for the use in advanced ovarian, fallopian tube, or primary peritoneal cancer …

When it comes to life sciences and patient outcomes, the UK’s destiny is inextricably tied to its relationship with the …

The FDA has granted marketing authorisation to Vertex’s Trikafta (elexacaftor/tezacaftor/ivacaftor and ivacaftor) for the treatment of cystic fibrosis (CF), it …

A small study has found that the commonly prescribed medication for kids and teenagers with autism is no more effective …