Injection Techniques of Collagenase Clostridium Histolyticum (CCH) for the Treatment of EFP (Cellulite)

Completed · Phase 2

Conditions studied: Edematous Skin

In brief

The study will evaluate the safety and effectiveness of different injection techniques of Collagenase Clostridium Histolyticum (CCH) for the treatment of adult women with mild, moderate or severe Edematous Fibrosclerotic Panniculopathy (commonly known as Cellulite).

Key facts

Study ID

NCT03632993

Run by

Endo USA Inc., a Keenova Therapeutics Company

People needed

64

Starts

2018-09-18

Expected to finish

2019-01-24

Last updated by the study team

2023-09-07

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• No participant will be assigned to treatment until all eligibility criteria have been satisfied. To qualify for the study a participant must:
• Be able to provide voluntary written informed consent prior to the initiation of any study specific procedures per the policy of the governing Institutional Review Board (IRB)/Independent Ethics Committee (IEC).
• Be female and at least 18 years of age at the time of consent.
• Have evidence of cellulite in 2 bilateral treatment areas (defined as right and left buttocks or right and left posterolateral thighs) as assessed by the Investigator at the Screening visit, and fulfills the following requirements:
• has a score of 2 (mild), 3 (moderate) or 4 (severe) as reported by the Investigator (CR-PCSS) in 2 treatment areas (two thighs or two buttocks) at the Screening Visit.
• has at least 2 dimples from each treatment area that:
• are isolated and separated by at least 5 centimeters (cm) from any other dimples.
• score 2 or 3 on the Hexsel depression scale.
• have dimple width: length ratio ≥ 0.5.
• Be willing to apply sunscreen to the dosing areas before each exposure to the sun while participating in the study (that is, screening through end of study).
• Be judged to be in good health, based upon the results of a medical history, physical examination, and laboratory profile at screening.
• Have a negative serum pregnancy test at the Screening Visit and negative urine pregnancy at Day 1 (before injection of study drug), be using an effective contraception method (for example, abstinence, intrauterine device, hormonal [estrogen/progestin] contraceptives, or double barrier control) for at least 1 menstrual cycle prior to study enrollment and through Day 71; or be menopausal defined as at least 12 months of amenorrhea in the absence of other biological or physiological causes (as determined by the Investigator), or be post-menopausal for at least 1 year, or be surgically sterile (hysterectomy, bilateral oophorectomy, bilateral tubal ligation).
• Be willing and able to comply with all protocol required study visits and assessments.

You may not qualify if…

• Participants who meet any of the following criteria will be excluded from the study:
• Is pregnant or is intending to become pregnant during the study.
• Is presently nursing/breastfeeding or providing breast milk.
• Has any of the following systemic conditions:
• Coagulation disorder.
• Evidence or history of malignancy (other than excised basal-cell carcinoma) unless there has been no recurrence in at least 5 years.
• History of keloidal scarring or abnormal wound healing.
• Concurrent diseases or conditions that might interfere with the conduct of the study, confound the interpretation of the study results, or endanger the participant's well-being.
• Evidence of clinically significant abnormalities on physical examination, vital signs, electrocardiogram (ECG), or clinical laboratory values.
• Has any of the following local conditions in the areas to be treated:
• History of lower extremity thrombosis or post-thrombosis syndrome.
• Vascular disorder (for example, varicose veins, telangiectasia).
• Inflammation or active infection.
• Severe skin laxity, flaccidity, and/or sagging.
• Active cutaneous alteration including rash, eczema, psoriasis, or skin cancer.
• Has a tattoo located within 2 cm of the site of injection.
• Requires anticoagulant or antiplatelet medication during the study or has received anticoagulant or antiplatelet medication (except for ≤ 150 mg aspirin daily) within 7 days before injection of study drug.
• Has used any of the following for the treatment of EFP on the area to be treated within the timelines identified below or intends to use any of the following at any time during the course of the study:
• Liposuction within the treatment areas during the 12-month period before injection of study drug.
• Injections (for example, mesotherapy); radiofrequency device treatments; laser treatment; or surgery (including subcision and/or powered subcision) within the treatment areas during the 12-month period before injection of study drug.
• Any investigational treatment for EFP/cellulite on treatment areas during the 12-month period before the injection of study drug.
• Endermologie® or similar treatments within the treatment areas during the 6-month period before injection of study drug.
• Massage therapy within the treatment areas during the 3-month period before injection of study drug.
• Creams (for example, Celluvera™, TriLastin®) to prevent or mitigate EFP within the treatment areas during the 2-week period before injection of study drug.
• Has received an investigational drug or treatment within 30 days before injection of study drug.

Where it is running

• Endo Clinical Trial Site #1 — Coral Gables, Florida, United States
• Endo Clinical Trial Site #5 — Miami, Florida, United States
• Endo Clinical Trial Site #2 — New York, New York, United States
• Endo Clinical Trial Site #4 — New York, New York, United States
• Endo Clinical Trial Site #3 — New York, New York, United States

Full record on ClinicalTrials.gov

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