Evidence on the clinical and cost effectiveness of Remdesivir is currently under review through the NICE multiple technology appraisal process.

Do not use remdesivir for COVID-19 pneumonia in anyone in hospital and on high-flow nasal oxygen, continuous positive airway pressure, non-invasive mechanical ventilation or invasive mechanical ventilation, except as part of an ongoing clinical trial.

 

Conditional recommendations:

- Consider a 3-day course of remdesivir for children and young people who weigh at least 40 kg and adults with COVID-19 who:

When assessing the person, take into account likely response to any vaccinations against COVID-19 they have already had, any comorbidities or risk factors, and whether their condition is deteriorating.

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- Consider a course of remdesivir (up to 5 days) for people who:

  • have COVID-19 pneumonia, and
  • are in hospital and need low-flow supplemental oxygen.

The criteria for accessing remdesivir in the UK are outlined in NHS England's Interim Clinical Commissioning Policy on remdesivir for people in hospital with COVID-19which includes people who are significantly immunocompromised.

For remdesivir use in pregnancy, follow the Royal College of Obstetrics and Gynaecology guidance on COVID-19 and pregnancy.

This recommendation is informed by the results of clinical trials that included very few people who had been vaccinated against COVID-19. Also, the trials took place before the emergence of the Delta (B.1.617.2) and Omicron (B.1.1.519) variants.

 

Adapted from NICE COVID-19 rapid guideline: Managing COVID-19 - Therapeutics for COVID-19