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Gilead's Remdesivir Results Encouraging, Safety Brings Skepticism

 
• By Joseph Haas

Analysts see NIAID’s placebo-controlled data as more important than Gilead’s open-label data. Quick emergency use authorization by FDA is possible, but the US agency has not confirmed EUA.

Happy Hopeful Woman Looking at the Sunset by the Sea. Silhouette of a dreamer girl looking hopeful at the horizon
Analysts and NIAID director Fauci called the data significant and reason for optimism

News from Gilead Sciences Inc. and the US National Institute of Allergy and Infectious Diseases on 29 April about remdesivir in the treatment of COVID-19 produced a wave of optimism throughout financial markets based on the first evidence of a treatment benefit in patients sickened by the novel coronavirus.

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Europe Pharma Heavyweights Call For Higher Drug Prices At Home

 
• By Kevin Grogan

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Galapagos Chief Exec Stoffels Leaving, While Firm Names Spinout’s CEO

 
• By Mandy Jackson

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MetaVia’s ‘Safe’ Obesity Drug Resonates With Analysts, But Not Investors

 
• By Joseph Haas

The biotech reported Phase I multiple-ascending dose data for its obesity drug for the second time in a week, but its safety and tolerability do not offset concerns about relatively unimpressive weight reduction.