EN3835 for the Treatment of Edematous Fibrosclerotic Panniculopathy (Commonly Known as Cellulite)

Completed · Phase 2 · Has a placebo group

Conditions studied: Edematous Fibrosclerotic Panniculopathy, Cellulite

In brief

The study will evaluate the safety, effectiveness, and immunogenicity of EN3835 in the treatment of adult women with Edematous Fibrosclerotic Panniculopathy (Commonly known as Cellulite).

Key facts

Study ID

NCT02724644

Run by

Endo USA Inc., a Keenova Therapeutics Company

People needed

375

Starts

2016-02-01

Expected to finish

2016-09-01

Last updated by the study team

2017-11-06

Who can join

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

You may qualify if…

• Be a female ≥18 years of age
• At Screening visit, have at least 1 quadrant with:
• a score of 3 or 4 (moderate or severe) as reported by the subject (PR- PCSS), and
• a score of 3 or 4 (moderate or severe) as reported by the Investigator (CR-PCSS), and
• a Hexsel CSS score no greater than 13
• At Day 1 visit, have an assigned quadrant with:
• a score of 3 or 4 (moderate or severe) as reported by the subject (PR-PCSS), and
• a score of 3 or 4 (moderate or severe) as reported by the Investigator (CR-PCSS), and
• a Hexsel CSS score no greater than 13
• Be willing to apply sunscreen to the selected treatment quadrant before each exposure to the sun while participating in the study (ie, 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 urine pregnancy test at screening and be using an effective contraception method (eg, abstinence, intrauterine device [IUD], hormonal [estrogen/progestin] contraceptives, or double barrier method) for at least 1 menstrual cycle prior to study enrollment and for the duration of the study; or be menopausal defined as 12 months of amenorrhea in the absence of other biological or physiological causes, as determined by the investigator; or post-menopausal for at least 1 year; or be surgically sterile.
• Be willing and able to cooperate with the requirements of the study
• Voluntarily sign and date an informed consent agreement approved by the Institutional Review Board/Independent Ethics Committee/Human Research Ethics Committee (IRB/IEC/HREC).
• Be able to read, complete and understand the Patient Reported Outcomes rating instruments in English

You may not qualify if…

• Has any of the following conditions:
• Thyroid disease, unless controlled with medication for ≥6 months
• Uncontrolled diabetes mellitus, as determined by the Investigator
• Uncontrolled hypertension, as determined by the Investigator
• Vascular disorder (eg, phlebitis or varicose veins) in area to be treated
• Cushing's disease and/or use of systemic corticosteroids at a total daily dose greater than 5 mg prednisone (or equivalent)
• History of lower extremity thrombosis or post-thrombosis syndrome
• Documented autoimmune disorder such as lupus erythematosus, rheumatoid arthritis
• Inflammation or active infection in area to be treated
• Active cutaneous alteration in area to be treated including rash, eczema, psoriasis or skin cancer
• History of keloidal scarring or abnormal wound healing
• Coagulation disorder
• Taking a medication for chronic anticoagulation (except for ≤150 mg aspirin daily)

Where it is running

• Clinical Testing of Beverly Hills — Beverly Hills, California, United States
• Dermatology Specialists, Inc — Murrieta, California, United States
• Dermatology Specialists, Inc — Oceanside, California, United States
• Dermatology Cosmetic Laser Medical Associates of LaJolla, Inc — San Diego, California, United States
• Olympian Clinical Research — Clearwater, Florida, United States
• Skin Research Institute LLC — Coral Gables, Florida, United States
• Research Institute of the Southeast — West Palm Beach, Florida, United States
• Mercy Health Research — Washington, Missouri, United States
• Bass Plastic Surgery, PLLC — New York, New York, United States
• Sadick Research Group — New York, New York, United States
• Dermatology Consulting Services — High Point, North Carolina, United States
• Tennessee Clinical Research Center — Nashville, Tennessee, United States
• Austin Institute for Clinical Research — Pflugerville, Texas, United States
• Charlottesville Medical Research Center LLC — Charlottesville, Virginia, United States
• The Education & Research Foundation — Lynchburg, Virginia, United States
• Premier Clinical Research — Spokane, Washington, United States

Full record on ClinicalTrials.gov

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