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A Study to Assess the Effectiveness of BOTOX (Botulinum Toxin Type A) Injections for the Change of Masseter Muscle Prominence in Adult Participants

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NCT06068855

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

Phase
Phase 3
Status
Completed
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
249actual
Sites
27
Countries
Belgium, Bulgaria, France +4

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
Start2023-10-17actualWhen the study began enrolling
Primary completion2025-11-20actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-11-20actualThe whole study's end, after follow-up
First posted2023-10-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-12-10actualThe 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 Botulinum Toxin Type A
  • Drug: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Achievement of 2-grade or more improvement from baseline on the Masseter Muscle Prominence Scale (MMPS) as assessed by the Investigator
measured Day 90
Achievement of 2-grade or more improvement from baseline on the Masseter Muscle Prominence Scale - Participant (MMPS-P) as assessed by the Participant
measured Day 90

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