shot-button
Maharashtra Elections 2024 Maharashtra Elections 2024
Home > News > India News > Article > Zydus receives emergency use approval for COVID 19 drug Virafin

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

Updated on: 23 April,2021 12:00 AM IST  |  Ahmedabad
IANS |

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

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

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.


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


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.

Earlier the Phase 2 clinical trials study established the early safety, efficacy and tolerability of Virafin and indicated that Pegylated Interferon alpha-2b had significant statistical clinical impact on the patient suffering from moderate Covid 19 disease by reducing their viral load helping in better disease management such as reduced duration of oxygen support.

This story has been sourced from a third party syndicated feed, agencies. Mid-day accepts no responsibility or liability for its dependability, trustworthiness, reliability and data of the text. Mid-day management/mid-day.com reserves the sole right to alter, delete or remove (without notice) the content in its absolute discretion for any reason whatsoever

"Exciting news! Mid-day is now on WhatsApp Channels Subscribe today by clicking the link and stay updated with the latest news!" Click here!


Mid-Day Web Stories

Mid-Day Web Stories

This website uses cookie or similar technologies, to enhance your browsing experience and provide personalised recommendations. By continuing to use our website, you agree to our Privacy Policy and Cookie Policy. OK