
New Phase 3 has been released by AstraZeneca, showing that the PD-L1 inhibitor Imfinzi (durvalumab), when combined with tremelimumab, failed …

New research has pinned a concrete figure on the perennial industry question: how much does it cost to bring a …

China has moved to authorise Roche’s Actemra (tocilizumab) as a treatment for severe complications from contracting the COVID-19 coronavirus in …

Takeda’s Alunbrig (brigatinib) has been recommended for approval by the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human …

Gilead has revealed it is to acquire the immunology firm Forty Seven in a deal valued at $95.50 per share …

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

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

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

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

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

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A federal judge in New York’s Southern District has ruled that 10 years of unpublished clinical trial data must now …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

A new report from the Scottish Government has revealed that the country’s life sciences sector is on track to breeze …