Russia seals another deal to supply and test its coronavirus vaccine abroad

vaccine me 1 1 - Russia seals another deal to supply and test its coronavirus vaccine abroad

Russia’s sovereign wealth fund will supply 100 million doses of its potential coronavirus vaccine to Indian drug company Dr Reddy’s Laboratories, the fund said on Wednesday, as Moscow speeds up plans to distribute its shot abroad.

The deal for its Sputnik-V vaccine candidate comes after the Russian Direct Investment Fund (RDIF) reached agreements with Indian manufacturers to produce 300 million doses of the shot in India, also a major consumer of Russian oil and arms.

The agreement brings the total number of doses Russia has so far announced that it will supply abroad to just over 200 million – half to Latin America and half to India. RDIF has said it has received requests totalling 1 billion doses.

Deliveries to India, which has a population of more than 1.3 billion, could begin in late 2020, RDIF said, adding this was subject to the completion of trials and Sputnik-V’s registration by regulatory authorities in India.

Phase III trials, involving at least 40 000 people, are ongoing in Russia. Initial results are expected in October or November, RDIF head Kirill Dmitriev has said.

Dr Reddy’s, one of India’s top pharmaceutical companies, will carry out Phase III clinical trials of Sputnik-V in India, RDIF said. Following the news, Dr Reddy’s shares rallied to close 4.18% higher in India on Wednesday.

The Indian trials could start as early as next month, Dmitriev told Reuters, adding trial results could be followed soon after by domestic regulatory approval of Sputnik-V for mass use in India.

India said last week it was considering granting an emergency authorisation for a coronavirus vaccine, particularly for the elderly and people in high-risk workplaces.

Russia was the first country to grant regulatory approval for a novel coronavirus vaccine and did so before large-scale trials were complete, stirring concern among scientists and doctors about the safety and efficacy of the shot.

Several countries are now considering adopting “emergency use authorisation” measures that would fast-track approval of a vaccine in a similar way, however.

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