
President Donald Trump is set to announce that Moncef Slaoui, the former head of GlaxoSmithKline’s vaccine division, and Gustave Perna, …

Public Health England (PHE) have approved Roche’s antibody test to help determine how much of the population has been infected …

The FDA has granted Fast Track designation for Moderna Inc’s mRNA vaccine candidate against the coronavirus. The regulatory body had …

AMAG Pharmaceuticals announced that it will cut 30% of its staff, or 140 jobs, as part of a companywide restructuring. …

Gilead Sciences has signed an exclusive licensing agreement with five generics drug companies in India and Pakistan to supply them …

Developments in treatments for COVID-19 continue to dominate the news as the latest in hydroxychloroquine trials shows it does not …

Scientists are studying if senicapoc, a treatment for sickle cell anemia, can be repurposed to mitigate damage to a COVID-19 …

Remdesivir, perhaps the leading hope in the race against COVID-19, has secured approval from Japan’s Ministry of Health, Labour and …

The FDA has given Emergency Use Authorisation for another COVID-19 diagnostics test for antibodies from Abbott Laboratories. With this approval, …

The Chinese city of Wuhan, where the coronavirus originated, plans to test all of its residents after 6 new cases …

The Phase 3 trial for Genfit’s drug elafibranor has failed to improve outcomes for patients with the fatty liver disease …

The FDA has provided new guidelines to researchers studying potential COVID-19 treatments to help speed up the process of their …

Dr LaRee Tracy, a lecturer at San Diego State University and Director of Biostatistics at PHASTAR, led a team of …

The European Commission has awarded marketing approval to Takeda’s subcutaneous formulation of its gut-selective biologic therapy Entyvio (vedolizumab) as a …

The results of another study into the use of hydroxychloroquine in COVID-19 patients has cast further doubts on its effectiveness …

Lynparza (olaparib), developed by AstraZeneca and MSD, has secured FDA approval when paired with bevacizumab as a first-line maintenance treatment …

The FDA has announced that Retevmo (selpercatinib) has been approved to treat both non-small-cell lung cancer (NSCLC) and medullary thyroid …

The US National Institute of Allergy and Infectious Diseases (NAID) has announced that it is enrolling COVID-19 patients in hospital …

NICE has revealed that it has recommended the NHS use of Roche’s Kadcyla (trastuzumab emtansine) for HER2+ breast cancer in …

A recent report from the Office of National Statistics has shown that black people in England and Wales are four …