Phase 4
N=58
Sequential Treatment With BELKYRA® Then Juvéderm® VOLUMA™ With Lidocaine for Overall Improvement in Jawline Contour
Contour
Bottom Line
View on ClinicalTrials.gov: NCT03425253 ↗Enrolled (actual)
58
Serious AEs
3.8%
Results posted
Dec 2020
Primary outcome: Primary: Percentage of Participants Who Showed ≥ 1-point Jawline Improvement From Baseline on the Allergan Loss of Jawline Definition Scale (ALJDS), as Assessed by the Investigator — 92.9; 92.9; 92.9 percentage of participants
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 4
- Interventions
- BELKYRA® (Drug); Juvéderm® VOLUMA™ with Lidocaine (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Allergan
- Primary completion
- Dec 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Participants Who Showed ≥ 1-point Jawline Improvement From Baseline on the Allergan Loss of Jawline Definition Scale (ALJDS), as Assessed by the Investigator |
92.9; 92.9; 92.9 | — |
| SECONDARY Mean Change From Baseline to Last BELKYRA® Treatment on the ALJDS |
2.7; -0.6; 2.5; -0.6; 2.6; -0.6 | <0.001 sig |
| SECONDARY Mean Change From Baseline to Final Study Visit in the FACE-Q™ Satisfaction With Lower Face and Jawline Score |
24.1; 55.9 | <0.001 sig |
| SECONDARY Mean Change From Baseline to Final Study Visit in the FACE-Q™ Appraisal of Neck |
13.8; -11.0 | 0.597 |
| SECONDARY Mean Change From Baseline to Final Study Visit for FACE-Q™ Appraisal of Area Under Chin |
60.1; -45.4 | <0.001 sig |
| SECONDARY Mean Change From Baseline to Final Study Visit for Clinician-Reported Submental Fat Rating Scale (CR-SMFRS) |
2.5; -1.9 | <0.001 sig |
| SECONDARY Mean Change From Baseline to Final Study Visit for Patient-Reported Submental Fat Rating Scale (PR-SMFRS) |
2.3; -1.6 | <0.001 sig |
| SECONDARY Mean Change From Baseline to Final Study Visit for Submental Skin Laxity Grade (SMSLG) Score |
2.0; -0.3 | 0.003 sig |
| SECONDARY Mean Change From Baseline to Final Study Visit in Jawline Definition, Based on Independent Reviewer Assessment Using the ALJDS and Photographic Images |
2.9; -0.7; 2.7; -0.5; 2.8; -0.9 | <0.001 sig |
Summary
This study has been designed to evaluate the safety and effectiveness of sequential treatment with BELKYRA® (for the treatment of convexity and fullness associated with submental fat) and VOLUMA™ (to restore volume along the mandibular border) to enhance the overall contour of the jawline.
Eligibility Criteria
Inclusion Criteria
- Grade 2 or above on Allergan Loss of Jawline Definition Scale (ALJDS)
- Grade 2 or 3 on reported Clinician-Rated Submental Fat Rating Scale (CR-SMFRS)
- Stable body weight for at least 26 weeks
- Accept the obligation to forego any treatment or behavior (e.g., unshaven facial hair; significant changes to dietary or exercise habits) during the participants participation in the study that may affect the assessments of the submental area
Exclusion Criteria
- Grade 4 on Submental Skin Laxity Grade (SMSLG)
- Grade 4 on Allergan Jowl Fat Rating Scale (AJFRS)
- Body mass index (BMI) >35 kg/m^2
- History of, or current symptoms of dysphagia
- History of temporary, semi-permanent or permanent facial or neck dermal filler injections below the medial canthi at any time prior to treatment, or within 52 weeks before Screening for treatment above the medial canthi
- History of facial and/or neck plastic surgery, tissue grafting or permanent facial implants anywhere in the face or neck
- History of any intervention (e.g., liposuction, surgery, or lipolytic agents) to treat submental fat (SMF)
- Evidence of any cause of enlargement in the submental area other than localized SMF
- History of mesotherapy or ablative procedures to the face and/or neck 52 weeks before Screening
- History of skin resurfacing in the neck or submental area within 26 weeks before Screening
- Treatment with botulinum toxin injections in the neck or submental area within 26 weeks before Screening
- Participants on prescription topical retinoid therapy and/or topical hormone cream applied to the face, who have not been on a consistent dose regimen for at least 26 weeks before Screening and who are unable to maintain regimen for the study
- Systemic retinoid therapy within 52 weeks before Screening
- Current use of oral corticosteroids
- Is on a regimen of anticoagulation therapy (eg, warfarin, clopidogrel)
- Has current injection site inflammatory or infectious processes, abscess, an unhealed wound, or a known cancerous or precancerous lesion in chin, masseter, or submental region
- Planned oral surgery or other dental procedures (e.g., tooth extraction, orthodontia, or implantation) within 2 weeks prior to and after VOLUMA™ treatment
Data sourced from ClinicalTrials.gov (NCT03425253). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.