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Dermatology Times is looking back on the top stories in dermatology from the month of June.
FDA Approves Expanded Use of Tirbanibulin for Actinic Keratosis
Phase 3 clinical trial results showed that the safety and tolerability profiles were consistent with those observed in the original pivotal trials.
MoonLake Immunotherapeutics Announces FDA, EMA Support of Furthering Phase 3 Sonelokimab for PsA
The phase 3 IZAR program will evaluate the efficacy and safety of sonelokimab in patients with psoriatic arthritis for a 1 year duration.
FDA Approves Tralokinumab Autoinjector for Adults With Moderate to Severe Atopic Dermatitis
LEO Pharma's Adbry, a single-dose autoinjector, is expected to become available to patients in the coming months.
Botanix Pharmaceuticals announced the approval of its sofpironium topical gel, 12.45% for adults and children ages 9 and older.
Authorization for Eli Lilly's Ebglyss is based on positive results from the ADvocate 1, ADvocate 2, and ADhere studies.
FDA Grants Investigational New Drug Clearance for Ensemble No.2 for Phase 1 Atopic Dermatitis Trial
Ensemble No.2, or ENS-002, is an investigational live biotherapeutic product first detected by Concerto Biosciences using its kChip technology.
Efficacy of Dupilumab in Treating Atopic Hand and Foot Dermatitis
The trial results indicated 3 significant improvements across all AHFD subtypes with dupilumab treatment compared to placebo.
Q&A: Alexa Kimball, MD, MPH, Talks BE HEARD Data for Hidradenitis Suppurativa
UCB recently announced phase 3 BE HEARD I and II trial results on bimekizumab for treating moderate to severe HS were published in The Lancet.
Phase 3 trials have been initiated in patients with high-risk melanoma.
Improvements in patient-reported outcomes were higher among patients treated with upadacitinib 30mg versus 15mg.
Roflumilast cream 0.15% is being evaluated for patients with mild to moderate atopic dermatitis down to 6 years.
The phase 3b/4 LEVEL-UP study assessed adolescents and adults with moderate to severe atopic dermatitis.
Late-Breaker: Positive 52-week Data for Rademikibart in Patients with AD
The data, presented at RAVE 2024, continued a positive trend, building upon strong phase 1 results of rademikibart for patients with AD.
Lebrikizumab Maintains EASI 90 Responses up to 38 Weeks After Discontinuation
The post-hoc analysis evaluated the relationship between lebrikizumab serum concentration levels and sustained clinical response after lebrikizumab discontinuation.
Upadacitinib Available for Pediatric Patients with pJIA, PsA
Upadacitinib is now available as a tablet or an oral solution for patients 2 years and older with pJIA as well as PsA.
VYNE Therapeutics Initiates Phase 2b Trial of BET Inhibitor VYN201 for Vitiligo
The primary efficacy endpoint is the proportion of subjects achieving at least a 50% improvement in the Facial Vitiligo Area Scoring Index.
First Patients Dosed with VYN202 for Inflammatory Diseases
VYNE Therapeutics Inc. shared that top-line data from the trial is expected in the second half of 2024.
Visual Racism and Racial Bias Persist in Dermoscopy Imaging
In one study, less than 5% of images from a HAM10000 database came from patients with darker skin types.
Individuals in Uyo, Nigeria, with albinism are at great risk of developing photodermatoses due to a lack of photoprotection and awareness of photoprotective behaviors.
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