Oral Nirmatrelvir-Ritonavir for Covid-19 in Higher-Risk Outpatients.
Summary
Oral Nirmatrelvir-Ritonavir for Covid-19 in Higher-Risk Outpatients. Original Article Abstract Background Nirmatrelvir-ritonavir has been shown to reduce progression to severe illness from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in unvaccinated high-risk outpatients. The effectiveness of nirmatrelvir-ritonavir in persons who have been vaccinated, infected naturally, or both is unclear. Methods In two open-label platform trials (PANORAMIC in the United Kingdom and C
Content
# Oral Nirmatrelvir-Ritonavir for Covid-19 in Higher-Risk Outpatients.
*Original Article*
# Abstract
## Background
Nirmatrelvir-ritonavir has been shown to reduce progression to
severe illness from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
in unvaccinated high-risk outpatients. The effectiveness of
nirmatrelvir-ritonavir in persons who have been vaccinated, infected naturally,
or both is unclear.
## Methods
In two open-label platform trials (PANORAMIC in the United Kingdom and
CanTreatCOVID in Canada), we enrolled higher-risk adults (≥50 years of age or
≥18 years of age with coexisting conditions) in the community who tested
positive for SARS-CoV-2 and had been unwell for 5 days or less. The participants
were randomly assigned to receive usual care plus nirmatrelvir (300
mg)-ritonavir (100 mg) twice a day for 5 days or to receive usual care alone.
The primary outcome was hospitalization or death from any cause within 28 days
after randomization.
## Results
From December 8, 2021, to September 30, 2024, a total of 3516
participants in the PANORAMIC trial and 716 participants in the CanTreatCOVID
trial underwent randomization. In the PANORAMIC trial, 14 of 1698 participants
(0.8%) in the nirmatrelvir-ritonavir group and 11 of 1673 participants (0.7%) in
the usual-care group were hospitalized or died (adjusted odds ratio, 1.18; 95%
Bayesian credible interval, 0.55 to 2.62; probability of superiority, 0.334). In
the CanTreatCOVID trial, 2 of 343 participants (0.6%) in the
nirmatrelvir-ritonavir group and 4 of 324 participants (1.2%) in the usual-care
group were hospitalized or died (adjusted odds ratio, 0.48; 95% Bayesian
credible interval, 0.08 to 2.23; probability of superiority, 0.830). In a
substudy involving 634 participants, viral load was reduced by the end of
treatment with nirmatrelvir-ritonavir. Serious adverse events with
nirmatrelvir-ritonavir were reported in 9 participants in the PANORAMIC trial
and in 4 participants in the CanTreatCOVID trial.
## Conclusions
In two open-label trials, nirmatrelvir-ritonavir did not reduce the
incidence of hospitalization or death among vaccinated higher-risk participants
with SARS-CoV-2 infection. (Funded by the National Institute for Health and Care
Research, and others; PANORAMIC ISRCTN number, 2021-005748-31; CanTreatCOVID
ClinicalTrials.gov number, NCT05614349.).
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DOI: 10.1056/NEJMoa2502457