
Bristol Myers Squibb has lifted the curtain on new Phase 3 data for its blockbuster immunotherapy Opdivo (nivolumab), showing that …

US firm Biogen is hoping for approval to bring about a treatment that could slow the onset of Alzheimer’s disease. …

Takeda has acquired licensing for a first-in-class investigational coeliac disease therapy CNP-101/TAK-101. The Japanese pharma giant now has the rights …

Porton Biopharma has signed a modification to its existing agreement with the US National Institute of Health’s National Institute of …

Novo Nordisk has celebrated the launch of a new Pharmatech A/S branch office based in Singapore at a grand opening …

Israeli drug company Teva has said that it would offer $250 million in cash and a supply of Suboxone, an …

Cancer Research UK has embarked on a new international alliance with a plan to develop ‘radical new strategies’ and technologies …

The US FDA has approved Trikafta (elexacaftor/ivacaftor/tezacaftor) – the first triple combination therapy available for patients with most common cystic …

Prime Minister Boris Johnson may have agreed a withdrawal agreement with the European Union at the 11th hour, but despite …

The FDA has moved to expand the existing label for Alexion’s Ultomiris (ravulizumab-cwvz) to include the treatment of atypical haemolytic …

The EMA’s human medicines committee (CHMP) has recommended seven medicines for approval at its October 2019 meet including MSD’s Ervebo, …

New Phase 3 data has emerged demonstrating the efficacy of Roche’s Tecentriq (atezolizumab) in combination with Avastin (bevacizumab) in the …

AstraZeneca have announced that the US FDA has approved Farxiga (dapagliflozin) to reduce the risk of hospitalisation for heart failure …

GlaxoSmithKline has announced it will divest two of its major vaccines to Denmark-based Bavarian Nordic in a deal that will …

This article follows parts one and two of our trio of in-depth pieces focusing on the growing medical cannabis phenomenon. …

It’s time for a rundown of the top 10 articles on PharmaFile this past week. The past seven days saw …

Fiscal year 2019 was a record-breaking one, according to the FDA. The US regulator smashed its previous total for annual …

The US FDA has recommended approval for cefiderocol, a novel antibiotic for complicated urinary tract infections, including pyelonephritis, in patients …

Roche subsidiary Genentech has announced that its polymerase acidic endonuclease inhibitor Xofluza (baloxavir marboxil) has been awarded FDA approval in …

MSD have announced it plans to eliminate approximately 500 jobs in multiple US states according to a filing with the …