Indian trials of the Sputnik-V vaccine candidate, being developed by
Russia's sovereign wealth fund, will enroll 1,000-2,000 participants
and be conducted at multiple government and private hospitals across
the country, Deepak Sapra, CEO for API and pharmaceutical services
at Dr. Reddy's, told Reuters.
"We want to get to the first step - which is the commencement of the
clinical trials by getting the necessary approvals from the Indian
regulators - within the next few weeks," Sapra said.
The trials are part of a deal between the Russian Direct Investment
Fund (RDIF) and Dr Reddy's, in which the Indian firm will conduct
Phase III studies in India, pursue local regulatory approvals and,
subject to approval, distribute the finished vaccine product in
India. RDIF will supply 100 million doses to Dr Reddy's.
The RDIF has also reached agreements with Indian manufacturers to
produce 300 million doses of the shot in India. Russia was the first
country to grant regulatory approval for a novel coronavirus
vaccine.
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Sputnik-V doses supplied in India will likely be a combination of Indian- and
Russian-made doses, Sapra said, adding that RDIF and Dr Reddy's would soon
identify potential manufacturers in India.
The RDIF has said vaccine deliveries to India could begin in late 2020, but
Sapra suggested it could take longer. "I think it's going to be several months
before we accomplish all the steps in the process," he added.
India, which has a population of more than 1.3 billion, is the world's second
worst affected country by COVID-19 behind the United States. For weeks, it has
reported the world's highest daily jump in infections, which reached a total of
5.6 million on Tuesday.
(Reporting by Sachin Ravikumar in Bengaluru; Editing by Shounak Dasgupta)
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