
Biopharmaceutical company Dunad Therapeutics (Dunad) has annouced that it has entered into a strategic collaboration with Novartis, to develop orally …

Novartis have announced that the FDA approved Scemblix® (asciminib) for the treatment of chronic myeloid leukaemia (CML) in two distinct …

A COVID vaccine skin patch is on course for its first human trial by the University of Queensland in partnership …

A US intelligence report saying it was plausible that COVID-19 originated in a Wuhan laboratory has been deemed unscientific and …

The FDA has informed Moderna that it needs more time to review the company’s COVID vaccine in children aged 12 …

The Russian Direct Investment Fund (RDIF, Russia’s sovereign wealth fund) has announced the results of a real world study by …

Gilead Sciences announced that it has entered into a clinical trial collaboration and supply agreement with MSD (known as Merck …

A Brazilian study has assessed the effect of early treatment with fluvoxamine on the risk of emergency care and hospitalisation …

Genentech have announced that Susvimo, previously known as the port delivery system, is the fist wet age-related macular degeneration (AMD) …

Clinical stage biopharmaceutical company, XBiotech, plans to test its new True Humanâ„¢ antibody therapy for reducing brain injury after stroke, …

Angel Pharmaceuticals has received approval for their IND application, from the Center for Drug Evaluation (CDE) of the China National …

The University of Texas MD Anderson Cancer Center has reported that Serial radiation therapy as monotherapy is a safe and …

ViiV Healthcare, the global specialist HIV company, have presented positive interim data showing Vocabria (cabotegravir) and Rekambys (rilpivirine), the first …

The FDA has approved Vitti Labs’ Investigational New Drug (IND) application to conduct Phase II Clinical Trials using a combination …

An advisor to the Department of Health told MPs a ‘Plan C’ has been mentioned in Government discussions, should the …

The MHRA has approved Quell Therapeutics’ first clinical trial for its lead cell therapy candidate QEL-001. This approval paves the …

A study conducted by Nature Medicine has revealed an increased risk of Guillain-Barre Syndrome (GBS) and Bell’s palsy following a …

The FDA and EMA have accepted Novartis’ Supplemental Biologics License Application (sBLA) and Type II Variation for KymriahⓇ in patients …

The National Institute for Health research has awarded funding to the University of Oxford, working with several other UK universities, …

The EMA’s human medicine’s committee (CHMP) has initiated a rolling review of the investigational antiviral drug molnupiravir for the treatment …