
Novartis’ Sandoz will pay a $195 million criminal penalty to resolve charges that it conspired to price-fix, rig bids and …

Sanofi’s monoclonal antibody and CD-38 inhibitor Sarclisa (isatuximab-irfc) has been awarded marketing authorisation from the FDA in the treatment of …

Most NHS doctors, that partcipated in a survey, feel the organization is not well prepared to deal with a major …

This article was originally published in the January/February 2020 issue of Pharmafocus.With the advent of a New Year, Michael Jewell, …

British firm GW Pharmaceuticals has revealed that it plans to reclaim the commercialisation rights to market its cannabis-based multiple sclerosis …

British Health Secretary Matt Hancock has said nothing will be “off the table” in tackling the coronavirus as cases in …

The FDA has awarded approval to the first generic medicine for the treatment of toxoplasmosis, authorising Cerovene’s version of Daraprim …

The Justice Department have announced that Sanofi SA have agreed to pay $11.85 million to resolve allegations it used a …

Results from a new study researching treatment for dyskinesia has offered hope that it may be treatable in people with …

Takeda’s subcutaneous formulation of its gut-selective biologic vedolizumab has secured recommendation from the European Medicines Agency’s (EMA) Committee for Medicinal …

The coronavirus continues to spread across the globe as the US launch their first trials for Gilead’s ebola drug remdesivir …

UK-based Acacia Pharma has secured its first US approval with the FDA’s decision to authorise Barhemsys (amisulpride injection) for the …

A person has been diagnosed with coronavirus in Wales, with the number of infected continuing to rise as numerous sporting …

A type of E. coli infection may increase a person’s chance of developing bowel cancer, according to a new study …

The latest monthly edition of Pharmafocus, the March issue, is available to read for free online now! The coronavirus continues …

Eli Lilly’s Cyramza (ramucirumab) has edged closer to US approval after it scored a recommendation from the FDA’s Oncologic Drugs …

NICE has chosen to recommend Celgene’s Revlimid (lenalidomide) for use on the NHS, it has emerged, alongside Genentech’s Rituxan (rituximab), …

The FDA’s Drugs Trials Snapshots 2019 report has been released, clarifying the demographic distribution of participants who were included in …

A federal judge in New York’s Southern District has ruled that 10 years of unpublished clinical trial data must now …

The first US clinical trial investigating a treatment for the COVID-19 coronavirus has been launched by the US National Institute …