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A Study to Learn if the Study Medicine Called Carbamazepine Changes How the Body Processes PF-07220060

← catalyst calendar

NCT06897683

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Basic science
Enrollment
14actual
Sites
1
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
Start2025-03-21actualWhen the study began enrolling
Primary completion2025-05-11actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-06-12actualThe whole study's end, after follow-up
First posted2025-03-27actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Adults

Interventions

  • Drug: PF-07220060
  • Drug: Carbamazepine ER Tablet

Primary outcomes

what the primary-completion date above is the date OF
Plasma PF-07220060 Maximum Observed Plasma Concentration (Cmax)
measured Pre-dose, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48, 72, 96 and 120 hours post-dose.
Plasma PF-07220060 Area under the plasma concentration versus time curve (AUC)
measured Pre-dose, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 8, 12, 16, 24, 36, 48, 72, 96 and 120 hours post-dose.

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