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A Trial to Learn if Different Doses of REGN17092 Are Safe in Healthy Adults

← catalyst calendar

NCT05923424

Sponsored by Regeneron Pharmaceuticals (industry) · REGN — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
40actual
Sites
1
Country
Belgium

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
Start2023-11-28actualWhen the study began enrolling
Primary completion2025-03-04actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-03-04actualThe whole study's end, after follow-up
First posted2023-06-28actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-03-27actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Volunteers

Interventions

  • Drug: REGN17092
  • Drug: Matching Placebo

Primary outcomes

what the primary-completion date above is the date OF
Occurrence of all treatment emergent adverse events (TEAEs)
measured Through approximately day 365
Severity of all TEAEs
measured Through approximately day 365
Occurrence of all treatment emergent serious adverse events (TE-SAEs)
measured Through approximately day 365
Severity of all TE-SAEs
measured Through approximately day 365

Posted documents

hosted by the registry — we link, never re-serve
Informed Consent Formposted 2023-08-01 · 370 KB · ICF_000.pdf

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