Wednesday, November 25, 2020

Sechnov University claims – Vaccine trial completed on two batches of volunteers, this is the second in the market

published on: 13/07/2020 4:56 AM

  • During the trial, it was seen whether the vaccine strengthens the immunity system of humans.
  • This vaccine has been prepared by the Russian Ministry of Defense and Gamlei National Research Center for Epidemiology.

Daily newspaper

Jul 12, 2020, 09:13 pm is

Moscow Russia claims to have prepared the Corona vaccine. Vadik Tarasov, director of Russia’s Sechnov University, said on Sunday that the clinical trial of the vaccine has been completed on two batches of volunteers. Of these, the first batch will be discharged on 15 July and the second batch on 20 July. During this trial, it was seen whether the vaccine strengthens the immunity system of the human body.

According to Alexander Lukashev, director of the University’s Institute of Medical Parasitology, Tropkill and Vector Born DCs, the vaccine has been found to be safe in the trial. It is safe like other vaccines in the market. Plans are being made to bring the new vaccine to market. It will be decided soon, given the state of the epidemic.

The vaccine trial started on 18 June

The university started the vaccine trial on 18 June. It has been prepared jointly by the Russian Ministry of Defense and the Gamlei National Research Center for Epidemiology. According to Russia’s Ministry of Defense, all volunteers attending the trial are feeling well. They are not experiencing any side effects. He was admitted to Burdenko Military Hospital, where the research protocol was fully followed.

Mardana Company has also tested vaccines on humans

The American company Mordana has also completed a human trial on the vaccine. The company completed the journey from getting the genetic code required for the vaccine to its trial in humans in just 42 days. It first began trials on humans before animals. The vaccine was first applied to a woman named 43-year-old Jennifer, a mother of two, at the Kaiser Permanente Research Facility in Seattle on March 16. The first trial included 45 healthy participants aged between 18 and 55 years old.

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