<p>Drug firm Glenmark Pharmaceuticals on Friday said that the addition of antiviral Umifenovir did not demonstrate any significant clinical benefit over Favipiravir alone in moderate Covid-19 patients.</p>.<p>The clinical study evaluated the possible superiority of the combination's efficacy against Favipiravir monotherapy, Glenmark said in a statement.</p>.<p><a href="https://www.deccanherald.com/national/coronavirus-news-live-updates-india-world-coronavirus-vaccine-karnataka-maharashtra-tamil-nadu-delhi-kerala-gujarat-bengal-bengaluru-mumbai-new-delhi-chennai-kolkata-cases-deaths-recoveries-AstraZeneca-Oxford-899419.html"><strong>For latest updates on coronavirus outbreak, click here</strong></a></p>.<p>As per the results that Glenmark presented to the regulator, the study showed no superior clinical outcomes with the addition of Umifenovir, it added.</p>.<p>This was the second clinical study after the successful Favipiravir monotherapy trial earlier this year that led the company to receive the Emergency Use Authorisation for Favipiravir, Glenmark said.</p>.<p>"These latest findings confirm that the addition of Umifenovir does not show any incremental benefit in clinical outcomes. Thus Favipiravir therapy along with supportive care remains a suitable and effective choice for mild to moderate Covid-19 infection," Monika Tandon Senior VP & Head, Clinical Development, Global Specialty/Branded Portfolio, Glenmark Pharmaceuticals said.</p>
<p>Drug firm Glenmark Pharmaceuticals on Friday said that the addition of antiviral Umifenovir did not demonstrate any significant clinical benefit over Favipiravir alone in moderate Covid-19 patients.</p>.<p>The clinical study evaluated the possible superiority of the combination's efficacy against Favipiravir monotherapy, Glenmark said in a statement.</p>.<p><a href="https://www.deccanherald.com/national/coronavirus-news-live-updates-india-world-coronavirus-vaccine-karnataka-maharashtra-tamil-nadu-delhi-kerala-gujarat-bengal-bengaluru-mumbai-new-delhi-chennai-kolkata-cases-deaths-recoveries-AstraZeneca-Oxford-899419.html"><strong>For latest updates on coronavirus outbreak, click here</strong></a></p>.<p>As per the results that Glenmark presented to the regulator, the study showed no superior clinical outcomes with the addition of Umifenovir, it added.</p>.<p>This was the second clinical study after the successful Favipiravir monotherapy trial earlier this year that led the company to receive the Emergency Use Authorisation for Favipiravir, Glenmark said.</p>.<p>"These latest findings confirm that the addition of Umifenovir does not show any incremental benefit in clinical outcomes. Thus Favipiravir therapy along with supportive care remains a suitable and effective choice for mild to moderate Covid-19 infection," Monika Tandon Senior VP & Head, Clinical Development, Global Specialty/Branded Portfolio, Glenmark Pharmaceuticals said.</p>