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A Study on Paxlovid Once in the Market, to Observe Its Safety and Effectiveness in Patients Who Have a High Chance of Getting Severe COVID-19

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NCT05890612 · readout in 912 d

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Status
Recruiting
Study type
Observational
Enrollment
3,000estimated
Sites
1
Country
South Korea

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-11-29actualWhen the study began enrolling
Primary completion2029-02-17estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-02-17estimatedThe whole study's end, after follow-up
First posted2023-06-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • COVID-19

Primary outcomes

what the primary-completion date above is the date OF
Proportion of patients with an adverse event (AE)
measured Baseline through Day 33
Proportion of patients with an adverse drug reaction (ADR)
measured Baseline through Day 33
Proportion of patients with a serious AE (SAE)
measured Baseline through Day 33
Proportion of patients with a serious ADR (SADR)
measured Baseline through Day 33
Proportion of patients with an unexpected AE (UAE)
measured Baseline through Day 33
Proportion of patients with an unexpected ADR (UADR)
measured Baseline through Day 33
Proportion of patients with a serious unexpected AE (SUAE)
measured Baseline through Day 33
Proportion of patients with a serious unexpected ADR (SUADR)
measured Baseline through Day 33
Proportion of COVID-19-related hospitalization from any cause
measured Baseline through Day 33
Proportion of COVID-19-related death from any cause
measured Baseline through Day 33
Proportion of subjective assessment of COVID-19-related symptomatic change
measured Day 5, Day 14, Day 33

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