A Study to Learn How Different Forms of the Study Medicine Called PF-08049820 Are Absorbed and Eliminated in Healthy Adults
← catalyst calendarNCT07597928 · readout in 15 d
Sponsored by Pfizer (industry) · PFE — their whole pipeline →.
Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
24estimated
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2026-05-13 | actual | When the study began enrolling |
| Primary completion | 2026-09-03 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2026-09-25 | estimated | The whole study's end, after follow-up |
| First posted | 2026-05-20 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-06-15 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Healthy Adults
- Healthy
Interventions
- Drug: PF-08049820
- Drug: Rabeprazole
Primary outcomes
what the primary-completion date above is the date OFArea under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUClast)
measured Baseline up to Day 16 for Part A and up to Day 24 for optional Part B
Area under the curve from time zero to extrapolated infinite time (AUCinf) if data permit
measured Baseline up to Day 16 for Part A and up to Day 24 for optional Part B
Maximum observed plasma concentration (Cmax)
measured Baseline up to Day 16 for Part A and up to Day 24 for optional Part B
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