FDA expands emergency use of Gilead’s remdesivir in hospitalised Covid-19 patients

WASHINGTON (REUTERS) – Gilead Inc said on Friday (Aug 28) the US Food and Drug Administration expanded the emergency use authorisation of its experimental antiviral Covid-19 treatment, remdesivir, to allow its use in all hospitalised Covid-19 patients.

The drug was authorised in May for use in patients with a severe form of the illness, after trial data showed the antiviral drug helped shorten hospital recovery time.

Remdesivir was first authorised in May 2020 for use in patients with a severe form of Covid-19.
Remdesivir was first authorised in May 2020 for use in patients with a severe form of Covid-19.PHOTO: REUTERS

Patients with more moderate Covid-19 were shown in studies to have modest benefit after being given the drug, according to a study published last week.

That study found that moderately ill patients treated with the antiviral drug for up to five days had significantly higher odds of improvement in certain areas, such as whether they needed supplemental oxygen, compared to patients given standard treatment.

But the importance of that benefit was uncertain, Gilead said, due to continued questions about how best to measure patient outcomes other than survival.

The FDA said in a press release that it had concluded that remdesivir may be effective to treat the disease and the potential benefits outweigh the risks.

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