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|February 3, 2009
FDA clears Lutronic’s AccuSculpt for laser-assisted lipolysis
Princeton Junction, N.J. - Lutronic has announced Food and Drug Administration clearance for their laser-assisted lipolysis system AccuSculpt, according to a company press release.
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Princeton Junction, N.J.
- Lutronic has announced Food and Drug Administration clearance for their laser-assisted lipolysis system AccuSculpt, according to a company press release.
The system is also indicated for the surgical incision, excision, vaporization, ablation and coagulation of soft tissue, according to the release, and for is the first and only pulsed Nd:YAG laser to deliver 1,444 nm wavelength for minimally invasive deep tissue heating.
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Phase 2 data presented at EADV 2026 showed daxdilimab significantly reduced disease activity and improved response rates in treatment-refractory DLE.
Presented as a late breaker at EADV 2026, mid-dose zumilokibart achieved EASI-75 in 65.9% of adults with atopic dermatitis vs 23.4% with placebo at week 16.
This review of the latest dermatological studies includes insights on ruxolitinib for lichen planus, early vitiligo treatment, psoriasis response, AD disease control, and PFB management.
EADV 2026 data highlight dupilumab’s effects on growth, quality of life, disease control, and itch across multiple dermatologic diseases.
The FDA approved therapies for melanoma, dermatomyositis, superficial basal cell carcinoma, and adolescent alopecia areata, while TYK2 inhibitors and rare disease filings advanced toward 2027 decisions.
Dermatology Times is looking back on the top stories in dermatology from the month of September.
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