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News: ETF warns that monoclonal antibodies may not be effective against emerging strains of SARS-CoV-2
Last updated: 09/12/2022nirmatrelvir / ritonavir) and Veklury (remdesivir), which have … COVID-19, including Paxlovid and Veklury, is available on EMA’s … Paxlovid)15 and Remdesivir (Veklury)16 that are approved in the … -
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News: Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 12-15 September 2022
CHMP, Last updated: 19/09/2022Veklury … -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 7-10 June 2022
PRAC, Last updated: 10/06/2022 -
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News: EMA adopts first list of critical medicines for COVID-19
Last updated: 08/06/2022 -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 4-7 April 2022
PRAC, Last updated: 08/04/2022 -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 7-10 March 2022
PRAC, Last updated: 11/03/2022 -
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News: Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 13-16 December 2021
CHMP, Last updated: 17/12/2021Veklury … -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 29 November - 2 December 2021
PRAC, Last updated: 03/12/2021 -
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News: COVID-19: EMA recommends authorisation of two monoclonal antibody medicines
CHMP, Last updated: 12/11/2021a positive opinion since Veklury (remdesivir) was recommended … -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 30 August – 2 September 2021
PRAC, Last updated: 17/09/2021 -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 7-10 June 2021
PRAC, Last updated: 11/06/2021of sinus bradycardia with Veklury The Pharmacovigilance Risk … -
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News: Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 17-20 May 2021
CHMP, Last updated: 21/05/2021marketing authorisation for Veklury renewed The Committee for … marketing authorisation for Veklury (remdesivir), the only authorised … considered that the benefits of Veklury continue to outweigh its … -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 3-6 May 2021
PRAC, Last updated: 07/05/2021 -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 8-11 March 2021
PRAC, Last updated: 12/03/2021 -
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News: EMA starts evaluating use of Veklury in COVID-19 patients not requiring supplemental oxygen
CHMP, Last updated: 23/02/2021EMA starts evaluating use of Veklury in COVID-19 patients not … application to extend the use of Veklury (remdesivir) to include treating … require supplemental oxygen. Veklury is currently authorised for … -
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News: Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 8-11 February 2021
PRAC, Last updated: 12/02/2021PRAC concludes that use of Veklury is not associated with kidney … 14 4.1.3. Remdesivir – VEKLURY (CAP … -
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News: Update on remdesivir - EMA will evaluate new data from Solidarity trial
Last updated: 20/11/2020in the EU in July 2020 as Veklury for the treatment of COVID-19 … require supplemental oxygen. Veklury was authorised on the basis … marketing authorisation of Veklury (remdesivir) in the EU. In … -
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News: Extra transparency measures for COVID-19 vaccines and therapeutics
Last updated: 30/10/2020of the authorisation of Veklury (remdesivir) and information … publication of clinical data for Veklury is in line with EMA’s … authorisation holder for Veklury. Health Canada is also publishing … -
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News: EMA starts first rolling review of a COVID-19 vaccine in the EU
Last updated: 01/10/2020of the COVID-19 medicine, Veklury (remdesivir … -
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News: Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 22-25 June 2020
CHMP, Last updated: 26/06/2020Veklury … -
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Press release: First COVID-19 treatment recommended for EU authorisation
Last updated: 25/06/2020marketing authorisation to Veklury (remdesivir) for the treatment … 25/06/2020 EMA/264817/2020 Generic Veklury: EPAR Veklury: Paediatric investigation …