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A Study to Compare S-217622 With Placebo in Non-Hospitalized Participants With COVID-19

← catalyst calendar

NCT05305547 · results posted

Sponsored by Shionogi (industry) · 4507.T — their whole pipeline →. With National Institute of Allergy and Infectious Diseases (NIAID).

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Randomized · Double · Treatment
Enrollment
2,093actual
Sites
196
Countries
Argentina, Brazil, Colombia +14

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 2026-08-20

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2022-08-03actualWhen the study began enrolling
Primary completion2024-01-07actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2024-05-24actualThe whole study's end, after follow-up
First posted2022-03-31actualWhen this record first appeared on the registry
Results posted2026-08-20actualWhen the sponsor posted results to the registry
Record updated2026-08-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • SARS-CoV-2 Infection

Interventions

  • Drug: S-217622
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Time to Sustained Symptom Resolution
measured Up to Day 29

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2023-10-25 · 924 KB · Prot_001.pdf
Statistical Analysis Planposted 2024-03-13 · 1.4 MB · SAP_002.pdf
Informed Consent Formposted 2023-03-10 · 443 KB · ICF_000.pdf

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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