Covid: US gives full approval for antiviral remdesivir drug

(BBC) – US regulators have given full approval for the antiviral drug remdesivir to treat Covid-19 patients in hospitals.

The US Food and Drug Administration (FDA) said Veklury, the drug’s brand name, cut the recovery time on average by five days during clinical trials.

“Veklury is the first treatment for Covid-19 to receive FDA approval,” the FDA said in a statement.

The World Health Organization (WHO) said last week remdesivir had little to no effect on patients’ survival.

The WHO said this was based on its own study – but the drug’s manufacturer Gilead rejected the findings of the trial.

Remdesivir had been authorised for emergency use only in the US since May.

In the US it will cost $3,120 via private insurers and $2,340 via government purchasers for a five-day course.

It was recently given to President Donald Trump after he tested positive for Covid-19. He has since recovered.

What did the FDA say?

In the statement, the FDA said the drug was approved on Thursday “for use in adult and paediatric patients 12 years of age and older and weighing at least 40 kilograms (about 88 pounds) for the treatment of Covid-19 requiring hospitalisation”.

“Today’s approval is supported by data from multiple clinical trials that the agency has rigorously assessed and represents an important scientific milestone in the Covid-19 pandemic,” said FDA Commissioner Stephen Hahn.

The regulator said its decision was supported by the analysis of data from “three randomised, controlled clinical trials that included patients hospitalised with mild-to-severe Covid-19”.

One of the studies showed that that “the median time to recovery from Covid-19 was 10 days for the Veklury group compared to 15 days for the placebo group”.