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A Study to Learn How Different Amounts of the Study Medicine Called PF-08049820 Are Tolerated and Act in the Body in Healthy Adults

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NCT06686797

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

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Double · Basic science
Enrollment
71actual
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
Start2024-11-27actualWhen the study began enrolling
Primary completion2026-02-23estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-02-23estimatedThe whole study's end, after follow-up
First posted2024-11-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-02-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy

Interventions

  • Drug: PF-08049820
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants With Treatment Emergent Adverse Events (TEAEs)
measured Baseline up to Day 35 of last dosing period for Parts A and C and up to Day 45 for Part B
Number of Participants With Serious Adverse Events (SAEs)
measured Baseline up to Day 35 of last dosing period for Parts A and C and up to Day 45 for Part B
Number of Participants With Clinically Significant Change From Baseline in Laboratory Abnormalities
measured Baseline up to Day 21 of last dosing period for Parts A and C and up to Day 31 for Part B
Number of Participants With Clinically Significant Change From Baseline in Vital Signs
measured Baseline up to Day 21 of last dosing period for Parts A and C and up to Day 31 for Part B
Number of Participants With Clinically Significant Change From Baseline in Electrocardiogram (ECG) Findings
measured Baseline up to Day 21 of last dosing period for Parts A and C and up to Day 31 for Part B

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