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		Russia's Sputnik V vaccine 91.6% effective in late-stage trial
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		 [February 02, 2021] 
		By Polina Ivanova 
 MOSCOW (Reuters) - Russia's Sputnik V 
		vaccine was 91.6% effective in preventing people from developing 
		COVID-19, according to peer-reviewed results from its late-stage 
		clinical trial published in The Lancent international medical journal on 
		Tuesday.
 
 Scientists said the Phase III trial results meant the world had another 
		effective weapon to fight the deadly pandemic and justified to some 
		extent Moscow's decision to roll out the vaccine before final data had 
		been released.
 
 The results, collated by the Gamaleya Institute in Moscow that developed 
		and tested the vaccine, were in line with efficacy data reported at 
		earlier stages of the trial, which has been running in Moscow since 
		September.
 
 "The development of the Sputnik V vaccine has been criticised for 
		unseemly haste, corner cutting, and an absence of transparency," 
		Professor Ian Jones of the University of Reading and Professor Polly 
		Roy, of the London School of Hygiene & Tropical Medicine, said in a 
		comment shared by The Lancet.
 
		
		 
		
 "But the outcome reported here is clear and the scientific principle of 
		vaccination is demonstrated," said the scientists, who were not involved 
		in the study. "Another vaccine can now join the fight to reduce the 
		incidence of COVID-19."
 
 The results were based on data from 19,866 volunteers, of whom a quarter 
		received a placebo, the researchers, led by the Gamaleya Institute's 
		Denis Logunov, said in The Lancet.
 
 Since the trial in Moscow began, there were 16 recorded cases of 
		symptomatic COVID-19 among people who received the vaccine, and 62 among 
		the placebo group, the scientists said.
 
 This showed that a two-dose regimen of the vaccine - two shots based on 
		two different adenovirus vectors, administered 21 days apart - was 91.6% 
		effective against symptomatic COVID-19.
 
 'RUSSIA WAS RIGHT'
 
 Russia approved the vaccine in August, before the large-scale trial had 
		begun, saying it was the first country to do so for a COVID-19 shot. It 
		named it Sputnik V, in homage to the world's first satellite, launched 
		by the Soviet Union.
 
 Small numbers of frontline health workers began receiving it soon after 
		and a large-scale roll out started in December, though access was 
		limited to those in specific professions, such as teachers, medical 
		workers and journalists.
 
 In January, the vaccine was offered to all Russians.
 
 "Russia was right all along," Kirill Dmitriev, head of the Russian 
		Direct Investment Fund (RDIF), which is responsible for marketing the 
		vaccine abroad, told reporters ahead of the publication of the results 
		on Tuesday.
 
 He said they supported Russia's decision to begin administering Sputnik 
		V to frontline workers while the trial was still underway, and suggested 
		scepticism of such moves was politically motivated.
 
 "The Lancet did very unbiased work despite some of the political 
		pressures that may have been out there," he said.
 
 The number of people vaccinated in Russia has remained low so far. 
		Authorities have pointed to some early issues with scaling up 
		production, while polls have shown low demand among Russians for the 
		vaccine.
 
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			A person receives an injection with Sputnik V (Gam-COVID-Vac) 
			vaccine against the coronavirus disease (COVID-19) at a hospital in 
			the village of Donskoye in Stavropol Region, Russia January 27, 
			2021. REUTERS/Eduard Korniyenko/File Photo 
            
			 
            Russia has already shared data from its Phase III trial with 
			regulators in several countries and has begun the process of 
			submitting it to the European Medicines Agency (EMA) for approval in 
			the European Union, Dmitriev said. 
            The data release comes as Europe scrambles to secure enough shots 
			for its 450 million citizens due to production cuts by AstraZeneca 
			and Pfizer while the U.S. roll-out has been hampered by the need to 
			store shots in ultra-cold freezers and uneven planning across 
			states.
 EFFECTIVE FOR ELDERLY
 
 There were 2,144 volunteers over 60 in the trial and the shot was 
			shown to be 91.8% effective when tested on this older group, with no 
			serious side-effects reported that could be associated with Sputnik 
			V, The Lancet summary said.
 
 The vaccine was also found to be 100% effective against moderate or 
			severe COVID-19, as there were no such cases among the group of 78 
			participants who were infected and symptomatic at 21 days after the 
			first shot was administered.
 
 Four deaths of participants occurred, but none was considered 
			associated with vaccination, The Lancet said.
 
 "The efficacy looks good, including in the over 60s," said Danny 
			Altmann, a professor of immunology at Imperial College London. "It's 
			good to have another addition to the global arsenal."
 
            
			 
			The authors of the study noted that because COVID-19 cases were only 
			detected when participants reported symptoms, further research is 
			needed to understand Sputnik V's efficacy on asymptomatic cases and 
			transmission.
 Sputnik V has been approved by 15 countries, including Argentina, 
			Hungary, and the United Arab Emirates and this will to 25 by the end 
			of next week, the RDIF's Dmitriev said.
 
 The sovereign wealth fund also said vaccinations using Sputnik V 
			will begin in a dozen countries, including Hungary, Bolivia, the 
			United Arab Emirates, Venezuela and Iran.
 
 However, large shipments of the shot have only been sent so far to 
			Argentina, which has received enough doses to vaccinate about 
			500,000 people, and Bolivia, which received 20,000 shots.
 
 Production for export will primarily be conducted by RDIF's 
			manufacturing partners abroad, the fund has said.
 
 On Tuesday, Dmitriev said that production had begun in India and 
			South Korea, and would launch in China this month. Trial doses have 
			also been produced by a manufacturer in Brazil.
 
 Russia is also conducting a small-scale clinical trial of a one-dose 
			version of the vaccine, which developers expect to have an efficacy 
			rate of 73% to 85%.
 
 (Additional reporting by Kate Kelland in London; Writing by Polina 
			Ivanova; Editing by Mark Potter and David Clarke)
 
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