Remdesivir approved for Covid-19 treatment in Singapore, Latest Singapore News - The New Paper

Remdesivir approved for Covid-19 treatment in Singapore

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Health Sciences Authority grants conditional approval to let infectious disease specialists give antiviral drug to some patients

Antiviral drug remdesivir can now be administered to seriously ill Covid-19 patients, making Singapore one of the few countries to get the nod to use it to treat the virus.

The Straits Times has learnt that the Health Sciences Authority (HSA) granted conditional approval yesterday to let infectious disease specialists give the drug to some patients.

Remdesivir, which is produced by US drugmaker Gilead Sciences, is the only treatment so far shown to benefit Covid-19 patients in a robust clinical trial.

Part of the conditional approval requires Gilead to collect safety data and to monitor the use of the drug. It must also submit data from ongoing clinical studies to HSA to ensure the safety and efficacy of the drug.

The HSA approval was obtained in less than three weeks after Gilead filed for registration of remdesivir on May 22.

"While the data on efficacy and safety is limited, the results from the clinical studies provided reasonable preliminary evidence to support a conditional approval," HSA told ST.

The approval is based on clinical data from the National Institute of Allergy and Infectious Diseases in the US' global phase three trial and another by Gilead, the firm said in a statement yesterday.


The National University Hospital (NUH) was one of the international sites for the Gilead-led trial. Singapore participated in both trials and enrolled about 100 patients, starting on March 12.

Remdesivir was previously available only in such clinical trials.

It is given as an intravenous injection to patients for five to 10 days and works by blocking an enzyme that is necessary for the Covid-19-causing virus to multiply.

It can be administered to patients with low oxygen saturation levels less than or equal to 94 per cent, or those who might require supplemental oxygen or more intensive breathing support such as extracorporeal membrane oxygenation (ECMO) or invasive mechanical ventilation.

ECMO is a type of life support involving a machine that takes over the role of the diseased lung and artifically oxygenates the blood outside the body.

While the drug has raised some concerns regarding side-effects on the liver, kidney and rashes during drug infusion, these seem to be contained, said Associate Professor Louis Chai, a senior consultant at the division of infectious diseases at NUH.

The HSA is working with the Ministry of Health (MOH) and relevant experts to further define the sub-category of patients likely to benefit most from this medicine, it said.

The MOH and the National Centre for Infectious Diseases (NCID) will develop guidelines on the appropriate use of the drug in healthcare institutions.

Infectious disease specialists will have access to remdesivir from the NCID.

The authorities are working closely with Gilead to secure supplies of the drug.