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Zydus receives emergency use approval for COVID-19 drug 'Virafin'

About 91.15 per cent of patients treated with the drug were RT-PCR negative by day seven, the company said in a statement.

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Prime Minister Narendra Modi at Zydus Biotech Park, a vaccine manufacturing facility in Ahmedabad. Pic/INDIAN PRESS INFORMATION BUREAU / AFP

Prime Minister Narendra Modi at Zydus Biotech Park, a vaccine manufacturing facility in Ahmedabad. Pic/INDIAN PRESS INFORMATION BUREAU / AFP

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.

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.

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