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A Study to Understand What the Body Does to the Study Medicine Called PF-07248144 When Taken by Healthy Adults

← catalyst calendar

NCT07423286

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Na · None · Basic science
Enrollment
8actual
Sites
2
Country
United States

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
Start2025-10-13actualWhen the study began enrolling
Primary completion2025-12-28actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-01-16actualThe whole study's end, after follow-up
First posted2026-02-20actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Adult Participants

Interventions

  • Drug: Oral [14C] PF-07248144
  • Drug: Oral unlabeled PF-07248144
  • Drug: IV [14C] PF-07248144

Primary outcomes

what the primary-completion date above is the date OF
Total recovery of radioactivity in urine, feces and vomitus (if any) expressed as a percent of total radioactive dose administered.
measured Period 1 pre-dose to maximum Days 22
Metabolic profiling/identification and determination of relative abundance of [14C]PF-07248144 and the metabolites of [14C]PF-07248144 in plasma, urine, and feces.
measured Period 1 pre-dose to maximum Days 22

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