Arabic Arabic English English French French German German

Gamaleya Research Institute of Epidemiology and Microbiology – Sputnik V

Candidate: Sputnik V

Category: VAX

Type: Vaccine consisting of two components, administered 21 days apart: Component 1 consists of a recombinant adenovirus vector based on the human adenovirus type 26, containing the SARS-CoV-2 S protein gene. Component 2 consists of a vector based on the human adenovirus type 5, containing the SARS-CoV-2 S protein gene. Both components are designed to enter human cells and produce an immune response. Immunity to SARS-CoV-2 will last for two years, according to Mikhail Murashko, Minister of Health of the Russian Federation.

Status: Russian President Vladimir Putin declared August 11 that his country’s regulators gave the world’s first regulatory approval to a COVID-19 vaccine that was developed by Gamaleya Research Institute of Epidemiology and Microbiology, run by the Health Ministry of the Russian Federation, despite the vaccine having no known Phase III trials according to the World Health Organization. Former FDA Commissioner Scott Gottlieb, MD, tweeted that the approval “may be another effort to stoke doubts or goad U.S. into forcing early action on our vaccines.”

Gottlieb and other observers also noted the low number of participants in the limited clinical study of the vaccine. According to, Sputnik V (under its old name of Gam-COVID-Vac) was tested in an open, two-stage, non-randomized Phase I/II trial (NCT04436471) that recruited just 38 participants, all healhy volunteers. The study’s primary outcome measures were the change in antibody levels against the SARS-CoV-2 glycoprotein S in 42 days; and the number of participants with adverse events.

The vaccine’s fast regulatory track prompted the resignation of Professor Alexander Chuchalin from the Russian Health Ministry’s ethics council. Chuchalin told Mail Online he challenged the two leaders in development of Sputnik V, Professor Alexander Gintsburg, Director of the Gamaleya Institute, and Professor Sergey Borisevich, a medical colonel and the Russian army’s top virologist: “Have you passed all the necessary paths approved by the Russian Federation legislation and the international scientific community? This job has not been done. Thus, one of the ethical principles of medicine has been grossly violated—to do no harm.”

Putin insisted the vaccine was safe: “I know that it works quite effectively, forms a stable immunity and, I repeat, has passed all the necessary tests.”

Putin also disclosed that one of his daughters had volunteered to take the vaccine, named for the first artificial Earth satellite that touched off the Cold War “Space Race” when launched in 1957 by the Soviet Union. She was said to have shown no side effects: “After the first vaccination, her temperature was 38 [degrees Celsius], the next day – 37 with a little and that’s it. . . . After the second injection, the second vaccination, the temperature also rose a little and then disappeared,” Putin said in remarks reported by the state-owned RIA Novosti news agency.

Gintsburgh told the Rossiya-1 television channel on August 16 that U.S. and European institutions had attempted to “poach” Gamaleya Institute researchers without success: “I would call it a natural negative reaction of Western companies to the emergence of a Russian production they did not expect. So, I think we should ignore these negative things that are being poured on us.”

Kirill Dmitriev, CEO of the $10 billion Russian Direct Investment Fund (RDIF), told the state-owned TASS news agency that clinical trials of Sputnik V were expected as of August 11 to start “soon” in the United Arab Emirates and the Philippines, where President Rodrigo Duterte has publicly expressed willingness to personally take the vaccine.

Dmitriev added 20 countries in Latin America, the Middle East, Asia, and elsewhere had requested to purchase from Russia a combined 1 billion doses. Manufacturing capacity was in place to produce 500 million doses, with plans for expansion, he added.

The vaccine will be administered to medical personnel, and then to teachers, on a voluntary basis by early September, with a mass roll-out in Russia expected to start in October, according to Reuters—though RIA Novosti said civil circulation of Sputnik V will start January 1, 2021, citing the state register of medicines of the Ministry of Health. The vaccine is to be produced at two sites: at the Gamaleya Center, and at the manufacturing site of Binnopharm.

Sputnik V underwent preclinical testing at the Gamaleya Center and 48 research institutes of the Ministry of Defense, followed by clinical studies at the Sechenov University and the branch of the Burdenko Main Military Clinical Hospital, RIA Novosti reported.

COVID-19: 200 Candidates and Counting

To navigate through the >200 potential therapeutic and vaccine options for COVID-19, GEN has grouped the candidates into four broad categories based on their developmental and (where applicable) clinical progress:

FRONT RUNNER – the most promising therapeutics/vaccines based on clinical progress, favorable data or both.

DEFINITELY MAYBE – earlier phases with promising partners, or more advanced candidates in development that have generated uneven data

KEEPING AN EYE ON… – interesting technology, attracting notable partners, or both, but preliminary data.

TOO SOON TO TELL – longshots pending additional experimental and/or clinical data.

GEN has also tagged the most common treatment types:



The post Gamaleya Research Institute of Epidemiology and Microbiology – Sputnik V appeared first on GEN – Genetic Engineering and Biotechnology News.

Read More

Leave a Reply

Your email address will not be published. Required fields are marked *

Previous Post

Novartis’ PD-1 combo flops in phase 3 melanoma test

Next Post

Piceatannol exerts anti-angiogenic efficiencies by blockage of vascular endothelial growth factor binding to its receptor.

Related Posts