Zydus drug Virafin gets DCGI nod, firm says it reduces need for oxygen support, recovery time
India TodayZydus Cadila has received emergency use approval from the Indian regulator for the use of its anti-viral drug 'Virafin'. Pharma giant Zydus says 91.15 per cent of adult patients treated with Virafin tested negative using RT-PCR in seven days. Virafin helps body cope with Interferon Alpha deficiency In its Phase III clinical trials, researchers found that a higher proportion of patients administered Virafin tested negative for the infection by the seventh day. What does clinical trial data for Virafin says It was found during the Phase III clinical trials of Virafin that patients administered the anti-viral drug showed considerable improvement on the eighth day as compared to the existing treatment for Covid-19 in moderate cases. In the Phase II clinical trials, Zydus found that there was a significant reduction of the viral load among Covid-19 patients treated with Virafin.