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Veklury (remdesivir)

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The pandemic and the pharmaceutical world

20 January 2021 | By Ezeokafor Ifeoma Charity (Remfall Healthcare)

Pharmacist Ezeokafor Ifeoma Charity explores to what extent COVID-19 has prompted the growth of the pharmaceutical industry.

news

EMA recommends 15 medicines for approval following December meeting

14 December 2020 | By Victoria Rees (European Pharmaceutical Review)

The EMA's human medicines committee has released its results for the December meeting, suggesting which therapies should receive marketing authorisation.

man with COVID-19 in a hospital bed, with an oxygen mask on with doctors checking his IV

news

Trial to compare dexamethasone and baricitinib in hospitalised COVID-19 patients

26 November 2020 | By Hannah Balfour (European Pharmaceutical Review)

The fourth iteration of the COVID-19 treatment trial will determine whether remdesivir plus baricitinib or dexamethasone is more effective at promoting recovery from COVID-19.

news

FDA approves remdesivir for treatment of COVID-19

23 October 2020 | By Victoria Rees (European Pharmaceutical Review)

The FDA has given marketing authorisation for Veklury (remdesivir) to treat COVID-19 patients requiring hospitalisation.

vials of remdesivir lined up next to a syringe and a bowl of cotton pads

news

EC signs a joint procurement contract for remdesivir

9 October 2020 | By Hannah Balfour (European Pharmaceutical Review)

The European Commission (EC) has signed a joint procurement contract to ensure an uninterrupted supply of Veklury (remdesivir) for participating countries.

news

FDA expands emergency use authorisation for remdesivir to treat all COVID-19 patients

1 September 2020 | By Victoria Rees (European Pharmaceutical Review)

The FDA has expanded the Emergency Use Authorisation for Veklury (remdesivir) to treat all hospitalised patients with COVID-19.

news

EMA recommends authorisation for remdesivir to combat COVID-19

25 June 2020 | By Victoria Rees (European Pharmaceutical Review)

The EMA's human medicines committee (CHMP) has recommended a conditional marketing authorisation for Veklury (remdesivir) to treat COVID-19.

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Recommended

Veklury (remdesivir)

The pandemic and the pharmaceutical world

EMA recommends 15 medicines for approval following December meeting

Trial to compare dexamethasone and baricitinib in hospitalised COVID-19 patients

FDA approves remdesivir for treatment of COVID-19

EC signs a joint procurement contract for remdesivir

FDA expands emergency use authorisation for remdesivir to treat all COVID-19 patients

EMA recommends authorisation for remdesivir to combat COVID-19