Zydus Cadila on Friday announced it has received restricted Emergency Use Approval from the Drug Controller General of India (DCGI) for the use of antiviral 'Virafin' in treating moderate COVID-19 infection in adults.
Virafin received emergency use approval for treating moderate COVID-19 infection in adults. The single dose subcutaneous regimen of the anti-viral drug reduced the need for supplemental oxygen, indicating that it was able to control respiratory distress and failure -- one of the major challenges in treating COVID-19, according to results of a multicentric trial conducted in 20-25 centres across India.
‘Virafin helps patients suffering from moderate COVID-19 disease by reducing their viral load, leading to a better disease management.’
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About 91.15 per cent of patients treated with the drug were RT-PCR negative by day seven, the company said in a statement. Read More..
The drug has also shown efficacy against other viral infections, it added. It will be available on the prescription of a medical specialist for use in hospital/institutional setup.
"The fact that we are able to offer a therapy which significantly reduces viral load when given early on can help in better disease management.
It comes at a much-needed time for patients and we will continue to provide them access to critical therapies in this battle against COVID-19," Dr Sharvil Patel, Managing Director, Cadila Healthcare Ltd, said in a statement.
In its Phase 3 clinical trials, the therapy showed better clinical improvement in the patients suffering from COVID-19.
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