Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Artefill (rebranded as Bellafill) is a permanent injectable dermal filler composed of 20% polymethylmethacrylate (PMMA) microspheres (30-50 microns in diameter) suspended in 80% purified bovine collagen gel, supplemented with 0.3% lidocaine for comfort. Developed by Suneva Medical (formerly Artes Medical), it was FDA-approved in 2006 for the correction of nasolabial folds and later for acne scars. The mechanism involves a dual-action approach: the bovine collagen provides immediate volume replacement, which is gradually replaced by the patient's own connective tissue as the non-resorbable PMMA microspheres act as a permanent scaffold to stimulate neocollagenesis. Dr. Gerald Pierone, Jr. has investigated the use of high-volume Artefill injections for the treatment of HIV-associated facial lipoatrophy, a condition characterized by the loss of facial fat due to antiretroviral therapy.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Artefill.