A Study to Evaluate Adverse Events and Effectiveness of OnabotulinumtoxinA in Participants Undergoing Open Abdominal Ventral Hernia Repair for the Achievement of Primary Fascial Closure Without the Use of Component Separation Technique
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Phase
Phase 2
Status
Withdrawn
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
0actual
Sites
2
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
Why the sponsor stopped it
Strategic considerations
As filed on the registry record, in the sponsor's own words.
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2024-05-07 | estimated | When the study began enrolling |
| Primary completion | 2025-04-22 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-09-26 | estimated | The whole study's end, after follow-up |
| First posted | 2022-11-07 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2024-05-16 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Ventral Hernia
- Abdominal Hernia
Interventions
- Drug: BOTOX Dose A — also filed as OnabotulinumtoxinA
- Drug: Placebo for BOTOX
- Drug: BOTOX Dose B — also filed as OnabotulinumtoxinA
- Drug: BOTOX Dose C — also filed as OnabotulinumtoxinA
Primary outcome
what the primary-completion date above is the date OFPercentage of participants with achievement of primary fascial closure (PFC) without the use of component separation techniques (CST) in open ventral hernia surgical repair
measured Up to 4 Months
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