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A Study to Learn About the Safety of PENBRAYA During Pregnancy

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NCT07768163 · readout in 2,080 d

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

Phase
Status
Recruiting
Study type
Observational
Enrollment
50estimated
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
Start2024-05-03actualWhen the study began enrolling
Primary completion2032-04-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2032-04-30estimatedThe whole study's end, after follow-up
First posted2026-08-17actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Meningococcal Disease

Intervention

  • Biological: PENBRAYA — also filed as PF-06886992

Primary outcomes

what the primary-completion date above is the date OF
Percentage of Major congenital malformations
measured Enrollment until 12 months after delivery
Percent of participants with spontaneous abortions
measured Enrollment until end of pregnancy (up to 20 gestational weeks)
Percent of participants with an elective termination.
measured Enrollment until end of pregnancy (up to 9 months)
Percent of participants with stillbirths
measured From start of pregnancy until 12 month post delivery between 05 March 2024 and 30 April 2032
Percent of participants with of preterm birth
measured Enrollment until 12 months after delivery
Percent of participants with children born small for gestational age (SGA)
measured Enrollment until 12 months after delivery

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