Glenmark Pharma announced that the addition of Umifenovir did not confirm any additional benefit over Favipiravir alone in moderate COVID-19 patients.
Addition of Umifenovir did not significantly benefit over Favipiravir alone in moderate COVID-19 patients, announced Glenmark Pharma. Umifenovir did not show superior clinical outcomes when added to Favipiravir treatment, and the trial did not meet the key endpoints.
‘Favipiravir therapy and supportive care remain a suitable and effective choice for treating mild to moderate COVID-19 infection.’
Glenmark on Friday announced the results of its "FAITH" combination trial with antivirals Umifenovir and Favipiravir for the treatment of moderate hospitalized Covid-19 patients. This was the second clinical study after the successful Favipiravir monotherapy trial earlier this year that led the company to receive the emergency use authorization for Favipiravir.
This second study, titled the FAITH trial evaluated the possible superiority of the
combination's efficacy against Favipiravir monotherapy.
As per the results that Glenmark presented to the regulator on Friday, the study showed no superior clinical outcomes with the addition of Umifenovir. The FAITH study enrolled in 158 hospitalized patients with moderate Covid-19 in India.
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The median time to clinical cure improved by only one day (7 as compared to 8) in patients who
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Commenting on the trial's findings, Monika Tandon, Senior Vice President, and Head, Clinical Development, Global Specialty/Branded Portfolio, Glenmark Pharmaceuticals Ltd., said, "Glenmark was the first company to provide patients an oral antiviral treatment for Covid-19 in India, and this combination study was yet another effort on our part to examine new treatment options to combat the health crisis.
"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."
Source-IANS