The official twitter account, promoting the Sputnik V COVID-19 vaccine, tweeted on 20 January 2021 that Russian Direct Investment Fund (RDIF), Russia's sovereign wealth fund, has filed for registration of the COVID-19 Sputnik V in the European Union and expects it to be reviewed in February 2021, Reuters news agency reported on Wednesday.
This moves the vaccine closer to a wider adoption across the globe.
The Sputnik V twitter account said that teams from the vaccine and the European Medical Agency (EMA) held a scientific review of the vaccine on 19 January 2021, adding that the EMA will take a decision on the authorisation of the vaccine based on the reviews.
RDIF's chief, Kirill Dmitriev, had said in an interview at the Reuters Next conference last week that Russia would submit a formal application to the European Union in February 2021 for approval of its Sputnik V COVID-19 vaccine.
Reportedly, the Sputnik V vaccine has already been approved in Argentina, Belarus, Serbia and other countries.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval