EpiVacCorona: Difference between revisions

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Latest revision as of 04:27, 18 February 2025

EpiVacCorona is a peptide-based vaccine against COVID-19 developed by the Vector Institute in Russia. It was authorized for emergency use in Russia in October 2020, following Phase I and II trials. As of March 2021, Phase III trials are ongoing.

Development[edit]

The Vector Institute, also known as the State Research Centre of Virology and Biotechnology, began development of EpiVacCorona in early 2020, following the global outbreak of the SARS-CoV-2 virus. The vaccine is based on synthetic peptide antigens of SARS-CoV-2 proteins, conjugated to a carrier protein and administered with an adjuvant.

Clinical Trials[edit]

EpiVacCorona underwent Phase I and II clinical trials in 2020. The trials involved a total of 100 participants and reportedly showed the vaccine to be safe and effective. However, the results have not been published in a peer-reviewed journal, leading to calls for greater transparency.

Phase III trials began in November 2020 and are expected to involve 3,000 participants. Preliminary results are expected in early 2021.

Efficacy[edit]

The Vector Institute has claimed that EpiVacCorona is 100% effective, based on the results of the Phase I and II trials. However, these claims have been met with skepticism due to the lack of published data.

Authorization[edit]

EpiVacCorona was granted emergency use authorization in Russia in October 2020, making it the second COVID-19 vaccine to be authorized in the country, after Sputnik V.

See Also[edit]


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