Johnson & Johnson applies for approval of its single-dose Covid vaccine in India

Global healthcare major Johnson & Johnson on Friday said it has applied for Emergency Use Authorization (EUA) of its single-dose COVID-19 vaccine in India. Earlier the company had said that it remained committed to bringing its single-dose COVID-19 vaccine to India and looks forward to ongoing discussions with the Indian government. The vaccine despite being declared by the US Centers for Disease Control and Prevention (CDC) that it had high efficacy at preventing hospitalisation and death in people ran into one hurdle after another.

“On August 5, 2021, Johnson & Johnson Pvt. Ltd applied for Emergency Use Authorisation (EUA) of its single-dose covid-19 vaccine to the Government of India,” read the statement.

Johnson & Johnson claimed that its single-shot vaccine, in clinical trials, proved to be 85 per cent effective in preventing severe disease. The vaccine also showed protection against Covid-19 related hospitalisation and death, it said.

“The EUA submission is based on topline efficacy and safety data from the Phase 3 ensemble clinical trial, which demonstrated our single-shot vaccine was 85 per cent effective in preventing severe disease across all regions studied, and showed protection against Covid-19 related hospitalisation and death, beginning 28 days after vaccination,” Johnson & Johnson said.

Johnson & Johnson further said Biological E will be an important part of its global supply chain network.

“This is an important milestone that paves the way to bringing our single-dose COVID-19 vaccine to the people of India, and the rest of the world, through a collaboration with Biological E. Limited. Biological E will be an important part of our global supply chain network, helping to supply our Johnson & Johnson Covid-19 vaccine through the extensive collaborations and partnerships we have with governments, health authorities and organisations such as Gavi and the COVAX facility,” the company said in a statement.

“We look forward to concluding our discussions with the government of India to accelerate availability of our COVID-19 vaccine to help end the pandemic,” the statement said.

If J&J’s vaccine gets approval in India, it will be the second foreign-made vaccine to be approved in the country, after Moderna.

India recorded 44,643 new coronavirus infections taking the total tally of COVID-19 cases to 3,18,56,757, while the active cases registered an increase for the third consecutive day, according to the Union Health Ministry data updated on Friday. The number of deaths climbed to 4,26,754 with 464 fresh fatalities.

By editor

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