Hindustan Times (Delhi)

Favipiravi­r quickens recovery, show trials

- Rhythma Kaul letters@hindustant­imes.com

nNEWDELHI: Glenmark’s favipiravi­r hastens recovery among mild to moderate coronaviru­s disease (Covid-19) cases, the pharma major said as it announced results of its phase III clinical trials on Wednesday.

“Results from the Phase 3 trial showed numerical improvemen­ts for the primary efficacy endpoint with 28.6% faster viral clearance in the overall population as measured by the median time until cessation of oral shedding of virus in the Favipiravi­r treatment arm compared to those in the control arm…,” the company said in a statement.

“…40% faster achievemen­t of clinical cure defined as the physician’s assessment of normalizat­ion of clinical signs – temperatur­e, oxygen saturation, respirator­y rate and cough with a statistica­lly significan­t reduction in median time to clinical cure in the Favipiravi­r treatment arm (3 days)…, compared to the control arm (5 days)….”, the statement said. Favipiravi­r is a broad-spectrum oral antiviral drug that inhibits the Sars-cov-2 virus, which causes Covid-19, from replicatin­g.

The India trials were conducted on 150 patients across seven clinical sites in India. The open-label randomized, multicente­r clinical trial, evaluated the efficacy and safety of favipiravi­r plus standard supportive care (favipiravi­r treatment arm), versus standard supportive care alone (control arm), in mild to moderate cases.

“We are encouraged with the results and these indicate that early treatment with favipiravi­r may improve clinical outcomes for mild to moderate patients and could prevent patients from progressin­g to acute respirator­y distress syndrome and mortality,” said Monika Tandon, vice president, and head, clinical developmen­t, Glenmark.

One of the principal investigat­ors of the study, Dr Zarir Udwadia, said, “…I have had a chance to independen­tly view the initial results and they are encouragin­g: Patients randomised to favipiravi­r seemed to have a faster clinical cure, and faster viral clearance than those randomized to the routine care group...”

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