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A Study to Assess BOTOX Injections for the Change of Masseter Muscle Prominence in Adult Participants

← catalyst calendar

NCT06399718

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
207actual
Sites
20
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
Start2024-04-30actualWhen the study began enrolling
Primary completion2025-11-10actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-11-10actualThe whole study's end, after follow-up
First posted2024-05-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Masseter Muscle Prominence

Interventions

  • Drug: BOTOX — also filed as OnabotulinumtoxinA
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Composite Achievement of MMP Severity Improvement and at Least a 2-Grade Improvement from Baseline by Both Investigator-Rated MMPS and Participant-Rated MMPS-P
measured Day 90
Number of Participants with Adverse Events (AEs)
measured Baseline to Day 360

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