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A Study to Learn How Different Amounts of the Study Medicine Called PF-07941944 Are Tolerated in the Body of Healthy Adults.

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NCT06920498

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

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
25actual
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
Start2024-12-03actualWhen the study began enrolling
Primary completion2025-06-19actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-06-19actualThe whole study's end, after follow-up
First posted2025-04-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-07-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy Participants

Interventions

  • Drug: PF-07941944
  • Drug: Placebo
  • Drug: Midazolam

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants With Treatment Emergent Treatment-Related Adverse Events (AEs)
measured Baseline through end of study, approximately 16 weeks
Number of Participants With Clinically Significant Change From Baseline in Laboratory Abnormalities
measured Baseline through end of study, approximately 16 weeks
Number of Participants With Clinically Significant Change From Baseline in Vital Signs
measured Baseline through end of study, approximately 16 weeks
Number of Participants With Change From Baseline in Electrocardiogram (ECG) Findings
measured Baseline through end of study, approximately 16 weeks
Maximum Observed Plasma Concentration (Cmax)
measured Baseline through end of study, approximately 16 weeks
Area Under the Curve From Time Zero to Extrapolated Infinite Time (AUCinf)
measured Baseline through end of study, approximately 16 weeks
Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast)
measured Baseline through end of study, approximately 16 weeks

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