Status:
COMPLETED
Study of Different Interventions to Reduce Bruising Following CCH-Aaes Treatment for Cellulite of the Buttocks
Lead Sponsor:
Endo Pharmaceuticals
Conditions:
Edematous Fibrosclerotic Panniculopathy
Cellulite
Eligibility:
FEMALE
18-60 years
Phase:
PHASE2
Brief 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 Q...
Detailed 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 additiv...
Eligibility Criteria
Inclusion
- Key
- Have a body mass index of 18 to \<32 kilograms (kg)/meter (m)\^2 and intends to maintain stable body weight during the study.
- Have both buttocks with moderate or severe cellulite as reported by the investigator using the Clinician Reported Photonumeric Cellulite Severity Scale (CR-PCSS).
- Have a Hexsel Cellulite Severity Scale (CSS) Total Score of ≤12.
- Has a Fitzpatrick Skin Type of I-IV
- Be willing to apply sunscreen to the treatment areas before each exposure to the sun for the duration of participation in the study.
- Be willing and able to comply with the requirements of the study.
- Key
Exclusion
- Has systemic conditions (coagulation disorders, skin pigmentation disorders, malignancy, keloidal scarring, abnormal wound healing) that restricts study participation.
- Is pregnant and/or is breast-feeding or plans to become pregnant and/or to breast-feed during the course of the study.
- Has any local (in the areas to be treated) conditions (thrombosis, post-thrombosis syndrome, vascular disorder, inflammation, active infection, active cutaneous alteration, tattoo or mole) that restricts study participation.
- Requires antiplatelet medication, anticoagulants, or non-steroidal anti-inflammatory drugs during the study.
- Any medications, supplements, or foods that have, or have been reported to have anticoagulant effects within 14 days of treatment.
- Has received treatment with investigational treatment within 30 days before treatment.
- Has used or intends to use any of the local applications, therapies, injections, or procedures for the treatment of cellulite on either buttock that would restrict study participation.
- Intends to initiate an intensive sport or exercise program or intensive weight reduction program during the study.
- Intends to engage in strenuous activity within 48 hours of study intervention administration.
- Has recently tanned or intends to tan (outdoors or indoors) during the study.
- Has a history of hypersensitivity or allergy to collagenase or any other excipient of CCH.
- Has any condition(s) that, in the investigator's opinion, might indicate the participant to be unsuitable for the study.
- Has participated in a previous investigational study of CCH or received any collagenase treatments at any time prior to treatment in this study for the treatment of cellulite of the buttocks.
- In addition to the applicable aforementioned exclusion criteria, participants enrolling in Cohort 7 will be excluded from study participation if the participant:
- Has any of the following medical conditions:
- history of venous or arterial thromboembolism or current thromboembolic disease.
- history of or current renal impairment.
- serum creatinine concentration \> 1.4 milligram/deciliter at Screening.
- Requires the following concomitant medications during the study and cannot discontinue these medications within the time specified before CCH-aaes treatment:
- concurrently taking combination hormonal contraceptives.
- concurrently undergoing hormone replacement therapy.
- is a current smoker of nicotine or cannabinoids.
- Participants in Cohort 7 should avoid smoking (including vaping, nicotine, or marijuana cigarettes) during the study.
Key Trial Info
Start Date :
June 15 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 21 2023
Estimated Enrollment :
91 Patients enrolled
Trial Details
Trial ID
NCT05419505
Start Date
June 15 2022
End Date
June 21 2023
Last Update
March 7 2025
Active Locations (13)
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1
Endo Clinical Trial Site #6
Scottsdale, Arizona, United States, 85255
2
Endo Clinical Trial Site #4
Beverly Hills, California, United States, 90210
3
Endo Clinical Trial Site #9
Encinitas, California, United States, 92024
4
Endo Clinical Trial Site #10
San Diego, California, United States, 92121