Injectable Poly‐l‐Lactic Acid for Human Immunodeficiency Virus–Associated Facial Lipoatrophy: Cumulative Year 2 Interim Analysis of an Open‐Label Study (FACES)
Background Studies of injectable poly‐l‐lactic acid (PLLA) in human immunodeficiency virus (HIV)‐associated facial lipoatrophy have predominantly included male Caucasians. Objective To report cumulative year 2 interim study results examining the safety and efficacy of injectable PLLA in subjects wit...
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Published in | Dermatologic surgery Vol. 38; no. 7pt2; pp. 1193 - 1205 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
01.07.2012
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Subjects | |
Online Access | Get full text |
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Summary: | Background
Studies of injectable poly‐l‐lactic acid (PLLA) in human immunodeficiency virus (HIV)‐associated facial lipoatrophy have predominantly included male Caucasians.
Objective
To report cumulative year 2 interim study results examining the safety and efficacy of injectable PLLA in subjects with HIV categorized according to Fitzpatrick skin type and sex.
Materials and Methods
This is an ongoing open‐label, multicenter, 5‐year study of 290 treated subjects. After correction with injectable PLLA, subjects are being followed annually. Primary end points include incidence and severity of treatment‐emergent adverse events (TEAEs). Secondary end points include mean change from baseline of James scale severity grade and treatment satisfaction.
Results
At 2 years, TEAE incidences were: potentially related to study product (n = 53,18.3%) or injection procedure (n = 71, 24.5%), injection‐site nodules (n = 24, 8.3%) and papules (n = 25, 8.6%). No hypertrophic scars, keloids, or product‐related serious TEAEs were reported. Mean improvement in James scale grade for all groups was 1.4 (p < .001), and 89.4% of subjects and 95.5% of physicians rated treatment satisfaction as very good or excellent.
Conclusion
At 2 years, injectable PLLA is a safe and effective long‐term treatment for HIV‐associated facial lipoatrophy regardless of Fitzpatrick skin type; confirmation of these results will be needed at the completion of this 5‐year study. |
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Bibliography: | This study was funded by Dermik Laboratories, a business of sanofi‐aventis U.S. LLC, A SANOFI COMPANY. All authors, with the exception of Elizabeth Daro‐Kaftan, PhD, were paid investigators. Editorial support was provided by Elizabeth Daro‐Kaftan, PhD, of Peloton Advantage, LLC. The authors were fully responsible for the content, editorial decisions, and opinions expressed in the current article. No author received an honorarium related to the development of this manuscript . ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 1076-0512 1524-4725 1524-4725 |
DOI: | 10.1111/j.1524-4725.2012.02474.x |