India approves emergency use of remdesivir to treat Covid-19 patients

BENGALURU - India's government said on Tuesday (June 2) it has approved Gilead Sciences's antiviral drug remdesivir for emergency use in treating Covid-19 patients.

Remdesivir is the first drug to show improvement in Covid-19 patients in formal clinical trials. It was granted emergency use authorisation by the US Food and Drug Administration last month and has received approval by Japanese health regulators.

"(Remdesivir) approved on June 1 under emergency use with condition for five dose administration," the Drugs Controller General of India said in an e-mail statement.

The drugmaker did not immediately respond to an e-mail seeking further details.

As of Tuesday, India has 198,706 cases of coronavirus and has recorded 5,598 deaths, health ministry data showed.

Gilead Sciences had on Monday reported that remdesivir showed modest benefit in patients with moderate Covid-19 given a five-day course, while those who received it for 10 days in the study did not fare as well.

European and South Korean authorities are also looking at remdesivir, with South Korean health authorities last Friday (May 29) saying they would request imports of the drug. Gilead is yet to gain regulatory approval in either market.

For the latest updates on the coronavirus, visit here.