Voluma Filler Agent For The Treatment of HIV-associated Facial Lipoatrophy

Jared Jagdeo, MD, MS

Status and phase: Completed; Phase 1

Conditions: HIV Facial Lipoatrophy

Treatments: Device: Voluma

Study type: Interventional

Funder types: Other; Other U.S. Federal agency; Industry

Identifiers

NCT02342223

Allergan-97727

Details and patient eligibility

About

The purpose of this study is to test the safety of Voluma and see what effects it has on HIV facial lipoatrophy. The hypothesis is that Voluma will be safe, efficacious and positively impact the quality-of-life in the treatment of facial lipoatrophy in patients with HIV.

Full description

HIV facial lipoatrophy (volume loss) is an increasing concern with patients on Highly Active Anti-Retroviral Therapy (HAART) because it affects the quality-of-life and adherence to medication regimen. Treatment of HIV facial lipoatrophy helps to improve patient wellness by removing the social stigma associated with HIV facial lipoatrophy. Currently, there are few medical therapies that can treat HIV facial lipoatrophy and are FDA-approved for this indication. Juvéderm Voluma (Allergan) may benefit patients on HAART because it may provide a more immediate aesthetic enhancement and potentially has fewer adverse effects, which results in a more natural appearing facial enhancement outcome. Voluma is the only agent that is FDA-approved for facial volume loss. We anticipate Voluma having less adverse effects than current FDA-approved drugs for HIV lipoatrophy as Voluma is a hyaluronic acid (HA)-based agent. The benefit of using hyaluronidase to "correct" or "modify" facial HA-based volume therapy is also a benefit for HIV patients, which currently does not exist as a post-injection modification option for other FDA-approved filling agents used to treat patients with HIV facial lipoatrophy. Voluma is currently FDA-approved for correction of age-related volume loss in the midface, and there's no alteration in the chemical or biophysical properties of Voluma that is being used in our proposed study. In addition to conventional injection techniques, we will implement the 'smile and fill' technique pioneered by our clinical research group to achieve better mid-face aesthetic outcomes.

Enrollment: 20 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Aged 18 years or more with laboratory evidence of HIV-1 infection and have been on HAART therapy for at least 1 (one) year.
• Not to have AIDS (CD4 count < 250) or AIDS-defining illness.
• Bilateral lipoatrophy corresponding to a visual grade 2 or above in the attached Carruthers Lipoatrophy Severity Scale (CLSS).
• Available and willing to attend study follow-up visits.
• Able and willing to give informed consent.

Exclusion criteria

• Any active skin inflammation or infection in or near the treatment area.
• Hypersensitivity to the components of Voluma.
• Previous treatment with Voluma or any other product for facial lipoatrophy within the past year.
• Has known bleeding disorder
• History of keloid formation
• Currently receiving systemic corticosteroids or anabolic steroids
• Currently on known anticoagulants (i.e. aspirin, non-steroidal anti-inflammatory drugs)
• Pregnancy or breastfeeding or anticipating becoming pregnant during the study period.
• Any other excluding factors that, according to the investigator's judgment, would preclude enrollment in the study.
• Any condition that may interfere with ability to comply with study requirements.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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20 participants in 1 patient group

Voluma

Experimental group

Description:

Subjects will be screened for severity on their HIV facial lipoatrophy according to the Carruthers Lipoatrophy Severity Scale (CLSS), and will receive subcutaneous injections of Voluma in the affected facial areas with the 'smile and fill' technique (Jagdeo 2014) based on Carruthers scoring scale. Subjects with Carruthers Score level 2 will receive total of 2-6 syringes of Voluma. Subjects with Carruthers Score level 3 will receive total of 4-8 syringes of Voluma. Subjects with Carruthers Score level 4 will receive total of 6-12 syringes of Voluma. All subjects will receive one Voluma treatment at initial time = 0 and may be eligible for touchup treatment, if necessary, at 2 weeks post-initial treatment.

Treatment:

Device: Voluma