Oman Daily Observer

Russia receives approval for Sputnik-v trials in India

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NEW DELHI/MOSCOW: The Russian Direct Investment Fund (RDIF) and Dr Reddy’s Laboratori­es Ltd have received renewed approval to conduct late-stage clinical trials in India of the Russian COVID-19 vaccine, the sovereign wealth fund said on Saturday.

Large-scale trials of the Sputnik-v vaccine in India were first announced and then knocked back by Indian regulators, who said the scale of Phase I and II trials conducted in Russia earlier this year was too small, requesting that they be repeated.

Following a new agreement, India will now carry out an adaptive phase II and III human clinical trial involving 1,500 participan­ts, RDIF, which is marketing the vaccine abroad, said on Saturday. Under the deal, Dr Reddy’s will conduct the clinical trials and, subject to approval, distribute the finished vaccine in India. RDIF will supply 100 million doses to Dr Reddy’s.

Russia, the first country to grant regulatory approval for a novel coronaviru­s vaccine, is also conducting Phase III trials of Sputnik-v in Belarus, Venezuela and the United Arab Emirates. RDIF has reached agreements with Indian manufactur­ers to produce 300 million doses of the shot.

A Phase III trial involving 40,000 participan­ts is currently underway in Moscow, with 16,000 people having already received the dose of the two-shot vaccine.

Interim results are expected to be published in early November.

Indian regulators have agreed to incorporat­e data, provided by Russia on a weekly basis, from the Moscow trial, a source close to the deal told Reuters.

Russia has also first reached an agreement with the biotechnol­ogy department of India’s Science and Technology Ministry to use its laboratori­es as a base for the Indian clinical trial, the source said.

The Indian government had begun identifyin­g about 300 million people who would be given the vaccine first when it is ready.

The Times of India said that frontline health and sanitation workers, police officials and elderly people with co-morbiditie­s will get the vaccine on priority.

The plan, which is still in the draft stage, aims to cover 23 per cent of the population in the first phase. The final plan is likely to be ready by end October-november, the report said.

— Reuters

 ?? — Reuters ?? India will now carry out an adaptive phase II and III human clinical trial involving 1,500 participan­ts.
— Reuters India will now carry out an adaptive phase II and III human clinical trial involving 1,500 participan­ts.
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