DA-13-007 Versus Sculptra for the Treatment of Nasolabial Folds Wrinkles

A Controlled, Randomized, Within-subject, Multi-center Prospective Clinical Trial of DA-13-007 (Injectable Poly-L-lactic Acid) Versus SCULPTRA® Aesthetic (Injectable Poly-L-lactic Acid) in the Treatment of Nasolabial Fold Wrinkles.

Study DA-13-007 is a randomized, evaluator-blinded, within subject (split face) multicenter clinical study of DA-13-007l (Injectable poly-l-lactic acid) compared to SCULPTRA in the treatment of nasolabial fold wrinkles. Qualifying subjects will be randomized to receive DA-13-007l and SCULPTRA on either the right or left side of the face.

Study Overview

• Status: Completed
• Conditions: Face; Atrophy
• Intervention / Treatment: Device: DA-13-007 right with left side Sculptra left side; Device: DA-13-007 left with left side Sculptra right side

Detailed Description

A randomized, evaluator-blinded, within subject (split face) multicenter clinical study of DA-13-007 (Injectable poly-l-lactic acid) compared to SCULPTRA in the treatment of nasolabial fold wrinkles. Qualifying subjects will be randomized to receive DA-13-007 and SCULPTRA on either the right or left side of the face. The treatment phase will consist of one to three visits at 3 week intervals during which eligible subjects will receive bilateral injections of study material in the left and right nasolabial fold wrinkles, including visits at weeks 3 and 6 for touch ups if needed. The follow-up phase will consist of assessments at 1, 3, 6, and 12 months after the last treatment, and safety and efficacy evaluations for an additional 12 months. Standardized photographs will be taken at screening and at all treatment phase and follow-up visits. Efficacy evaluations will be made by an on-site blinded evaluator, and of the photographs using a validated, standardized photo-numeric scale. The primary efficacy comparison between study treatments will be made on the mean change from baseline in the Wrinkle Severity Rating Scale of the nasolabial folds (as determined by the on-site blinded evaluator) and at the 12 month time point. Study participants will continue to be followed for safety and efficacy at months 18 and 24 after their last injection session.

• Study Type: Interventional
• Enrollment (Actual): 161
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Florida
    • Bradenton, Florida, United States, 34209
      • Bay Area Dermatology
    • Coral Gables, Florida, United States, 33146
      • Miami Skin Institute
  • Indiana
    • Carmel, Indiana, United States, 46032
      • Laser & Skin Surgery Center of Indiana
  • Washington
    • Spokane, Washington, United States, 99202
      • PCR

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 17 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• 1. Outpatient, male or female subjects of any race 21 years or older. Female subjects of childbearing potential must have a negative urine pregnancy test result at the Baseline Visit (test must have a sensitivity of at least 50U/mL for human chorionic gonadotropin) and practice a reliable method of contraception throughout the study.

  1. A female is considered of childbearing potential unless she is

     • postmenopausal for at least 12 months prior to study drug administration;
     • without a uterus and/or both ovaries; or
     • has been surgically sterile for at least 6 months prior to study drug administration.

  2. Reliable methods of contraception are:

     • hormonal methods or intrauterine device in use >30 days prior to study drug administration; or
     • barrier methods plus spermicide in use at least 14 days prior to study drug administration

     • vasectomized partner at least 3 months post operative or a zero sperm count post operatively 2. Demonstrate clinical evidence of moderate to severe bilateral aging in the nasolabial area, with wrinkles classified as a grade 3 or grade 4 on a 5-grade WSRS.

       3. Committed to abstain from procedures interfering with the treatment outcome (exclusion criteria) throughout the study.

       4. Able to understand the requirements of the study and sign Informed Consent and Photography Release forms.

Exclusion Criteria:

1. Pregnant (positive urine pregnancy test), are planning to become pregnant during the study period, have an infant they are breast-feeding, or who are of childbearing potential and not practicing a reliable method of birth control.
2. Subjects planning a facial cosmetic procedure during the study period or with prior cosmetic procedures (i.e., surgery) or visible scars that may affect the evaluation of response and/or quality of photography.
3. Facial asymmetry, ptosis, excessive dermatochalasis, deep dermal scarring, thick sebaceous skin, or an inability to substantially lessen upper facial rhytids even by physically spreading them apart.
4. Active skin disease within the treatment area within 6 months prior to study entry.
5. History of malignancy, excluding non-melanoma skin cancer within the past 5 years.
6. Profound atrophy/excessive weakness of muscles in target areas of injection.
7. History of facial nerve palsy.
8. Facial wrinkles therapy, such a permanent or enduring dermal fillers in the previous 2 years or bioresorbable during the previous 12 months.
9. Allergy or sensitivity to any component of the study medication (Section 8.1), or a known sensitivity to local anesthetics.
10. Previous botulinum toxin therapy within six (6) months of the Baseline Visit.
11. Use of systemic prednisone, penicillamine, anti metabolites or other bioequivalent collagen production inhibitors within 3 months of the Baseline Visit.
12. Has received (or is planning to receive) anti-coagulation, anti-platelet, or thrombolytic medications (e.g., warfarin), anti-inflammatory drugs (oral/injectable corticosteroids or non-steroidal anti inflammatory, eg.,aspirin, ibuprofen), or other substances known to increase coagulation time (e.g., Vitamin E, garlic, gingko). To clarify, no non-steroidal anti inflammatory e.g. asprin or ibuprofen within 10 days prior to injections or 3 days post injection.
13. Evidence of recent alcohol or drug abuse.
14. Medical and/or psychiatric problems that, in the Investigator's opinion, is severe enough to interfere with the study results.
15. History of poor cooperation, non-compliance with medical treatment, or unreliability.
16. Participation in an investigational drug or investigational device study within 3 months of the Baseline Visit.
17. A history of connective tissue disease (rheumatoid Arthritis, arthritis, lupus).
18. A history of multiple severe allergies or a history of anaphylactic shock.
19. Patients with a known history of or susceptibility to keloid formation or hypertrophic scarring.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Right Side DA-13-007, Left Side Sculptra; DA-13-007 right with left side Sculptra left side	Device: DA-13-007 right with left side Sculptra left side; The treatment phase will consist of one to three visits at 3 week intervals during which eligible subjects will receive bilateral injections of study material in the left and right nasolabial fold wrinkles, including visits at weeks 3 and 6 for touch ups if needed
Active Comparator: Left Side DA-13-007, Right Side Sculptra; DA-13-007 left with Sculptra right side	Device: DA-13-007 left with left side Sculptra right side; The treatment phase will consist of one to three visits at 3 week intervals during which eligible subjects will receive bilateral injections of study material in the left and right nasolabial fold wrinkles, including visits at weeks 3 and 6 for touch ups if needed

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Efficacy of treatment vs Comparator (using a 5-grade WSRS (wrinkle severity rating scale) score and a rating by an independent evaluator)	To evaluate the efficacy of treatment versus the comparator in a non-inferiority statistical model using a 5-grade WSRS (wrinkle severity rating scale) score and a rating by an independent evaluator	One Year

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
To evaluate the Global aesthetic improvement as assessed by investigators and subjects	• To evaluate the Global aesthetic improvement (GAI) as assessed by investigators and subjects	Two Year
To evaluate subjects satisfaction using a six point subject satisfaction questionnaire.	To evaluate subjects satisfaction using a six point subject satisfaction questionnaire.	Two Year

Collaborators and Investigators

• Sponsor: DermAvance
• Investigators: Principal Investigator: William Werschler, MD, Premier Clinical Research

Study record dates

Study Major Dates

• Study Start (Actual): January 1, 2015
• Primary Completion (Actual): December 1, 2018
• Study Completion (Actual): December 1, 2018

Study Registration Dates

• First Submitted: December 3, 2014
• First Submitted That Met QC Criteria: December 5, 2014
• First Posted (Estimated): December 8, 2014

Study Record Updates

• Last Update Posted (Actual): August 1, 2024
• Last Update Submitted That Met QC Criteria: July 31, 2024
• Last Verified: July 1, 2024

More Information

Terms related to this study

• Keywords: Nasolabial Folds
• Additional Relevant MeSH Terms: Pathological Conditions, Anatomical; Atrophy; Physiological Effects of Drugs; Natriuretic Agents; Diuretics, Osmotic; Diuretics; Mannitol
• Other Study ID Numbers: DermAvance DA-13-007

Drug and device information, study documents

• Studies a U.S. FDA-regulated device product: Yes