Pharma News

Paion’s ‘ultra-short-acting’ anaesthetic Byfavo has received approval from the UK Medicines and Healthcare products Regulatory Agency (MHRA) for use in procedural sedation.

Gilead has filed its investigational long-acting HIV drug lenacapavir with the US Food and Drug Administration (FDA), seeking approval in patients with multi-drug resistant infection.

Researchers investigating new diabetes treatments believe they have found evidence indicating excess production of a key neurotransmitter in the liver could be a key causal factor in the onset of insu...

Amid a reorganization scheme aimed at slashing costs and prioritizing immunology blockbuster Dupixent, Sanofi is hiving off a clutch of consumer brands sold mainly in Europe.

TEL AVIV, Israel & ZURICH--(BUSINESS WIRE)--Teva Pharmaceutical Industries Ltd.

JUN 28, 2021.

The UK health department recorded the emergence of the Lambda variant of COVID-19 , even as Delta Plus and Delta variants continue to remain a cause of concern in India and abroad.

The Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) granted breakthrough device designation for a deep brain stimulation (DBS) system (...

The monoclonal antibody Actemra (tocilizumab) was approved for emergency use in hospitalised paediatric and adult COVID-19 patients based on results from four clinical trials.

Eli Lilly has announced that its investigational GIP and GLP-1 inhibitor tirzepatide showed superiority over Novo Nordisk’s Ozempic in a Phase III trial.

Washington — Arkansas Governor Asa Hutchinson said Sunday he believes final, non-emergency use approval from the Food and Drug Administration (FDA) of coronavirus vaccines would help combat ...

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