Backyard species in US gets Covid-19 through human-to-animal spread
The SARS-CoV-2 virus was detected in six backyard species in the southeastern US state of Virginia with unique viral mutations with lineages closely.
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Wegovy gets EU regulator backing on lowering heart risks in obese people
The European Medicines Agency has backed Novo Nordisk’s Wegovy to expand the weight-loss drug’s application to lower heart risks and strokes in non-diabetic.
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Biogen, Sage halt tremor trial after ‘disappointing’ oral drug results
An oral investigational drug jointly developed by Biogen Inc., and Sage Therapeutics Inc., failed to stop essential tremors in patients, forcing the companies.
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Merck’s experimental RSV injection lowers infections in infants
The US-based Merck and Co.’s investigational medicine to protect infants from respiratory syncytial virus (RSV) disease has resulted in lowering infections, according to.
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US-based Agilent Technologies to acquire Canada’s Biovectra for $925m
HQ Team July 23, 2024: Agilent Technologies Inc., will acquire Canada-based Biovectra, a contract development and manufacturing company, for $925 million, according to.
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Conduct disorder in youth stems from changes in brain structure: NIMH
Conduct disorder is a result of extensive changes in the structure of the brain and is most noticeable in the cerebral cortex, or.
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AstraZeneca acquires France’s Amolyt Pharma for $1.05 billion
British-Swedish AstraZeneca has acquired Amolyt Pharma for $1.05 billion to gain access to Lyon, France-based company’s rare disease, late-stage pipeline.
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Pharmacy benefit managers in the US wielding ‘enormous power’: FTC report
Pharmacy benefit managers, who handle about 95% of US prescriptions, are inflating drug costs and squeezing independent pharmacies, according to a report.
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Bird flu detected in a fourth person in the US, health agency CDC says
The national public health agency of the US has reported a fourth person who was infected in the country with the highly pathogenic.
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FDA rejects Daiichi, Merck, antibody-drug conjugate application
The USFDA has rejected a Biologics License Application from Daiichi Sankyo and Merck & Co., seeking accelerated approval of patritumab deruxtecan to treat.