Before starting human clinical trials for the vaccine, pre-clinical studies on different animal species have been completed at all stages.
Phase 1 and 2 clinical trials of the vaccine were completed on August 1, 2020 According to the study results, no unforeseen or undesirable side effects were observed, and all volunteers felt well. It was found that the vaccine stimulates a strong antibody and cellular immune response.
The result of clinical studies conducted after the vaccine was administered showed no COVID-19 infection was in any of the participants. High sensitivity tests for antibodies in the blood serum of volunteers (including analysis for antibodies that neutralize the coronavirus) and the generation of both antibodies and cellular immune responses, which reveal the ability of the volunteers' immune cells to activate against the spiky S protein of the coronavirus, confirmed the high efficacy of the vaccine.
On August 25, 2020, clinical trials began involving more than 31,000 people in Russia and Belarus. However, countries such as the United Arab Emirates, India, and Venezuela have also locally participated in Sputnik V's clinical trials. On August 11, it was confirmed that the vaccine, which received approval from the Russian Ministry of Health, could be used to vaccinate the population in Russia under emergency rules adopted during the COVID-19 outbreak.
Phase 1 and 2 clinical trials of the vaccine were completed on August 1, 2020. Sputnik V showed strong efficacy, immunogenicity, and safety results in Phase III clinical trials.
The vaccine, which had mild side effects (94%) including flu-like symptoms, injection site reactions, headache and asthenia, showed an excellent safety profile.
The study, which found 91.6% efficacy against COVID-19, is based on an analysis of data from 19,866 volunteers who received both doses of the Sputnik V vaccine or placebo.
The Lancet confirmed the effectiveness of Sputnik V with published internationally peer-reviewed data.
The efficacy of the vaccine, which did not differ statistically from the ages 18-60 group, was observed as 91.8% in the age over 60 group.
The antibody level of patients recovering from COVID-19 was observed to be 1.3-1.5 times lower than the level of virus-neutralizing antibodies in the volunteers vaccinated with Sputnik V.
* Open Study on the Safety, Tolerance, and Immunogenicity of "Sputnik V Lyo" Vaccine Against COVID-19
* Open Study on Safety, Tolerance and Immunogenicity of "Sputnik V" Vaccine Against COVID-19
* Study on Efficacy, Safety and Immunogenicity of Sputnik V COVID-19 Vaccine Against COVID-19 (RESIST)
* Neutralizing Activity of Sera from Sputnik V-Vaccinated People against Variants of Concern (VOC: B.1.1.7, B.1.351, P.1, B.1.617.2, B.1.617.3) and Moscow Endemic SARS-CoV-2 Variants
* Sputnik Light booster after Sputnik V vaccination induces robust neutralizing antibody response to B.1.1.529 (Omicron) SARS-CoV-2 variant