Up to 91% of patients reached EASI-75 and up to 67% reached IGA 0/1 at week 152, with no new safety signals, according to Galderma's EADV 2026 data.
|Articles|November 4, 2008
Artes Medical announces enrollment reached for post-marketing study of ArteFill
San Diego - Artes Medical has announced enrollment is completed in the 1,000-patient post-marketing study required by the Food and Drug Administration for ArteFill, the only FDA-approved non-resorbable dermal filler, according to Business Wire.
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San Diego - Artes Medical has announced enrollment is completed in the 1,000-patient post-marketing study required by the Food and Drug Administration for ArteFill, the only FDA-approved non-resorbable dermal filler, according to Business Wire.
Study participants will be assessed for long-term nasolabial fold reduction and the safety profile of ArteFill over a five-year period. They will also rate their satisfaction with the treatment.
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