Details about the advantages of the human adenoviral vector vaccines are published on the “Sputnik V” website

Press release, 20.08.2020

Moscow, August 20, 2020 – The Russian Direct Investment Fund (RDIF), Russia’s sovereign wealth fund, and the Gamaleya National Research Institute of Epidemiology and Microbiology have launched an information section about the human adenovirus vaccine platform on the website of the world's first registered vaccine against coronavirus, “Sputnik V”, at: sputnikvaccine.com

The section contains links to scientific publications on the history of vaccines based on human adenoviruses and human adenoviral vectors, their clinical trials, the technological platform, the proven safety of this approach, as well as their application in the fight against various diseases.

Next week a previously planned post-registration, randomized, double-blind, placebo-controlled multicenter clinical study of the efficacy, immunogenicity and safety of the Sputnik V vaccine will begin in Russia, simultaneously with the vaccination of volunteers from risk groups. More than 40,000 people will take part in the study in more than 45 medical centers.

Please find a table comparing human adenovirus vaccines with other developments and key facts below.

  Human adenovirus Chimpanzee adenovirus mRNA
Approved antiviral drugs based on the specified platform 3 vaccines against Ebola: Over 60,000 people vaccinated (African states, China, Russia) NO NO
Approved cancer drugs based on the specified platform 2 cancer drugs: Over 30,000 people vaccinated (China) NO NO
Years since the beginning of the mass use of drugs based on this platform 17 years (cancer drugs) Not in use Not in use
Long-term safety studies (including no risk of carcinogenicity and reduced fertility) of drugs completed or underway YES NO NO
Full-scale production track record YES NO NO
Number of clinical trials completed in phase 3 - verification of safety, efficacy and therapeutic effect 4 0 0
Number of clinical trials on this platform 254 67 165
Number of people involved in completed clinical trials Over 20,000. Less than 7,000. Less than 10,000.
Number of people potentially involved in upcoming clinical trials Over 500,000. Less than 50,000. Less than 100,000.
Number of research papers on each platform 353 134 109

Clinical trials statistics are based on data from clinicaltrials.gov based on search queries containing platform names human adenoviral vector (Ad5, Ad26, etc.), chimpanzee adenoviral vector (ChAd3, ChAd63, etc.) and mRNA vaccine.

Statistics on research papers are based on pubmed.ncbi.nlm.nih.gov data searched by queries containing platform names.

Key facts

  • Research on human adenoviruses as a potential base for vaccine development began in 1953.
  • Vaccines do not contain live human adenoviruses, but human adenovirus vectors, that is, human viruses that cannot multiply in the body and are completely safe.
  • More than 20,000 people have taken part in clinical trials of vaccines and drugs based on human adenoviruses or human adenoviral vectors.
  • Human adenovirus vaccines have been used most widely by the US Army since 1971 to date. These type of vaccines are offered by the US Armed Forces to recruits. US Food and Drug Administration (FDA) approved human adenovirus vaccines in 2011. More than 10 million US military personnel have received the human adenovirus vaccines.
  • An anti-cancer drug based on human adenoviral vectors has been used to treat more than 30,000 patients in China.
  • Human adenovirus vaccines proven to have no long-term health risks, including no risk of carcinogenicity and no risk of affecting fertility. Health safety has been proven by more than 75 international publications and in more than 250 clinical trials.
  • Other means of delivering viral genetic material to stimulate the body's immune response, such as monkey adenovirus or mRNA technology, have never been used in approved vaccines before. No long-term studies have been conducted on the possible effects of such technologies for human body, including the possibility of cancer and the effect on fertility.
  • The approach of the Gamaleya Institute with the vaccine using two human adenoviruses serotypes: number 5 (Ad5) and number 26 (Ad26) has a clear advantage over the one-vector approach used by other developers.
  • Human adenoviral vectors are used in the development of vaccines against coronavirus by the world's leading pharmaceutical companies. At the same time, their vaccines are single-vector: CanSino (China) uses the Ad5 vector, which has already been approved for use by the Chinese army, Johnson & Johnson (USA) uses the Ad26 vector. Johnson & Johnson has received orders for more than 140 million doses of the drug based on the vector Ad26 from the United States and Europe.

Kirill Dmitriev, CEO of the Russian Direct Investment Fund, said:

“We get a lot of questions about the vaccine, including the platform on which it was developed. RDIF and the Gamaleya Institute strive for maximum transparency about the details of the vaccine’s development, which is why we post all information about adenovirus vaccines at sputnikvaccine.com. We would like to thank everyone for their interest in “Sputnik V” both in Russia and abroad - the vaccine website has already been visited by representatives of more than 200 countries. We plan to add new content to the site with new details on the vaccine in the future.”

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Russian Direct Investment Fund (RDIF) is Russia's sovereign wealth fund established in 2011 to make equity co-investments, primarily in Russia, alongside reputable international financial and strategic investors. RDIF acts as a catalyst for direct investment in the Russian economy. RDIF’s management company is based in Moscow. Currently, RDIF has experience of the successful joint implementation of more than 80 projects with foreign partners totaling more than RUB1.9 tn and covering 95% of the regions of the Russian Federation. RDIF portfolio companies employ more than 800,000 people and generate revenues which equate to more than 6% of Russia’s GDP. RDIF has established joint strategic partnerships with leading international co-investors from more than 18 countries that total more than $40 bn. Further information can be found at www.rdif.ru

For additional information contact:

Arseniy Palagin                                       Andrew Leach / Maria Shiryaevskaya
Russian Direct Investment Fund                        Hudson Sandler
Press Secretary                                        Tel: +44 (0) 20 7796 4133 
Tel: +7 495 644 34 14, ext. 2395
Mobile: +7 916 110 31 41
E-mail: arseniy.palagin@rdif.ru