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Study of Different Interventions to Reduce Bruising Following CCH-Aaes Treatment for Cellulite of the Buttocks — APHRODITE  

Cellulite Clinical Trial

Official title:
APHRODITE-1: A Phase 2, Open Label, Self-Controlled Study of Different Interventions to Reduce Bruising Following CCH-Aaes Treatment for Cellulite of the Buttocks in Adult Females

Clinical Trial Summary

The study will evaluate the effect of different doses, strengths (concentrations), diluent additives, depths of injection, and methods of injection on the severity of bruising potentially induced by QWO (collagenase clostridium histolyticum-aaes [CCH-aaes]).

Clinical Trial Description

The study will comprise a Screening Period (28 days), Treatment Period (90 days), and Follow-up Period (90 days). Participants will receive CCH-aaes in different doses, concentrations, diluent additives, depths of injection, and methods of injection in a split buttock arrangement, with the right buttock serving as the control, and the left buttock (investigational side) receiving a study intervention. ;

Study Design

Related Conditions & MeSH terms

  • Cellulite
  • Edematous Fibrosclerotic Panniculopathy
Clinical Trial Details
NCT number NCT05419505
Study type Interventional
Source Endo Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date June 15, 2022
Completion date June 21, 2023
View Details
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