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Gilead's Remdesivir Receives the US FDA's Emergency Use Authorization for the Treatment of COVID-19

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Gilead's Remdesivir Receives the US FDA's Emergency Use Authorization for the Treatment of COVID-19

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  • The EUA is based on two global P-III studies assessing 5-day & 10-day dosing durations of remdesivir (IV) vs PBO in patients with mod. to sev. symptoms of COVID-19- including those who are critically ill. Multiple additional clinical studies are ongoing to evaluate the safety and efficacy of remdesivir as a treatment for COVID-19
  • Under EUA- the 10-day & 5-day dosing regimen is for the patients requiring & not requiring invasive mechanical ventilation and/or ECMO respectively. If a patient on the 5-day dosing regimen does not demonstrate clinical improvement after 5days- treatment may extend for up to 5 additional days
  • The EUA will expedite broader use of remdesivir to treat hospitalized patients with severe COVID-19- enabling access to remdesivir at additional hospitals across the US

Click here ­to­ read full press release/ article 

Ref: Gilead | Image: Gilead

Related News:   Gilead Reports Results of Remdesivir in P-III SIMPLE Studies for Patients with Severe COVID-19


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This content piece was prepared by our former Senior Editor. She had expertise in life science research and was an avid reader. For any query reach out to us at connect@pharmashots.com

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