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

Inclusion Criteria:

No subject will be assigned to treatment until all eligibility criteria have been
satisfied. To qualify for the study a subject must:

1. 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).

2. Be female and at least 18 years of age at the time of consent.

3. 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:

1. 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.

2. has at least 2 dimples from each treatment area that:

- are isolated and separated by at least 5 cm from any other dimples.

- score 2 or 3 on the Hexsel depression scale.

- have dimple width: length ratio ≥ 0.5.

4. Be willing to apply sunscreen to the dosing areas before each exposure to the sun
while participating in the study (ie, screening through end of study).

5. Be judged to be in good health, based upon the results of a medical history, physical
examination, and laboratory profile at screening.

6. 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 (e.g., 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).

7. Be willing and able to comply with all protocol required study visits and assessments.

Exclusion Criteria:

Subjects who meet any of the following criteria will be excluded from the study:

1. Is pregnant or is intending to become pregnant during the study.

2. Is presently nursing/breastfeeding or providing breast milk.

3. Has any of the following systemic conditions:

1. Coagulation disorder.

2. Evidence or history of malignancy (other than excised basal-cell carcinoma)
unless there has been no recurrence in at least 5 years.

3. History of keloidal scarring or abnormal wound healing.

4. Concurrent diseases or conditions that might interfere with the conduct of the
study, confound the interpretation of the study results, or endanger the
subject's well-being. Any questions about concurrent diseases should be discussed
with the Medical Monitor.

5. Evidence of clinically significant abnormalities on physical examination, vital
signs, electrocardiogram (ECG), or clinical laboratory values.

4. Has any of the following local conditions in the areas to be treated:

1. History of lower extremity thrombosis or post-thrombosis syndrome.

2. Vascular disorder (eg, varicose veins, telangiectasia).

3. Inflammation or active infection.

4. Severe skin laxity, flaccidity, and/or sagging.

5. Active cutaneous alteration including rash, eczema, psoriasis, or skin cancer.

5. Has a tattoo located within 2 cm of the site of injection.

6. 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.

7. 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:

1. Liposuction within the treatment areas during the 12-month period before
injection of study drug.

2. Injections (eg, 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.

3. Any investigational treatment for EFP/cellulite on treatment areas during the
12-month period before the injection of study drug.

4. Endermologie® or similar treatments within the treatment areas during the 6-month
period before injection of study drug.

5. Massage therapy within the treatment areas during the 3-month period before
injection of study drug.

6. Creams (eg, Celluvera™, TriLastin®) to prevent or mitigate EFP within the
treatment areas during the 2-week period before injection of study drug.

8. Has received an investigational drug or treatment within 30 days before injection of
study drug.

9. Has a known systemic allergy to collagenase or any other excipient of study drug.

10. Has a history of drug or alcohol abuse.

11. Intends to initiate an intensive sport or exercise program during the study.

12. Intends to initiate a weight reduction program during the study.

13. Intends to use tanning spray or tanning booths during the study.

14. Has previously received any collagenase treatments (eg, Santyl® ointment and/or
XIAFLEX/XIAPEX®).

15. Was a subject in a previous cellulite clinical trial of EN3835: AUX-CC-830,
AUX-CC-831, EN3835-102, EN3835-104, EN3835-201, EN3835-202, EN3835-205, EN3835-302, or
EN3835-303.

16. Any other condition(s) that, in the Investigator's opinion, might indicate the subject
is unsuitable for the study.