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Combining Systemic Therapies in Psoriasis and Atopic Dermatitis

Dermatology Times

James Song, MD, explains combination treatment efficacy, addresses comorbidities, and provides pearls to improve patient safety.

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New Ladder Helps Guide Choice of Non-steroidal Treatments in AD

The Dermatology Digest

A newly developed therapeutic ladder can help guide dermatologists and patients on the use of nonsteroidal treatment options for atopic dermatitis (AD). The new topical therapies constitute the lower rungs of the therapeutic ladder and can be used for both exacerbations and maintenance. The study appears in Dermatitis.

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LEVEL UP Period 2 Data: AD Patients Who Switched From Dupilumab to Upadacitinib Hit Higher Treatment Targets

The Dermatology Digest

Atopic dermatitis (AD) patients who switched to upadacitinib (Rinvoq, AbbVie) from dupilumab (Dupixent, Regeneron, and Sanofi) hit higher treatment targets, according to results from Period 2 of the LEVEL UP study. The most frequently reported TEAEs included nasopharyngitis, acne, upper respiratory tract infection, and atopic dermatitis.

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FDA, EMA Accept Galderma’s BLA for Nemolizumab for PN and AD

The Dermatology Digest

Food and Drug Administration (FDA) has accepted Galderma’s Biologics License Applications for nemolizumab for the treatment of patients with prurigo nodularis (PN) and for adolescents and adults with moderate to severe atopic dermatitis (AD). Galderma is planning for multiple regulatory submissions in 2024.

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FDA Green Lights Leo’s Adbry for Kids With AD

The Dermatology Digest

Food and Drug Administration (FDA) has expanded the approval of tralokinumab-ldrm (Adbry, LEO Pharma Inc) to include kids aged 12-17 years with moderate-to-severe atopic dermatitis (AD) whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable.

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FDA Green Lights Leo’s Adbry for Kids With AD

The Dermatology Digest

Food and Drug Administration (FDA) has expanded the approval of tralokinumab-ldrm (Adbry, LEO Pharma Inc) to include kids aged 12-17 years with moderate-to-severe atopic dermatitis (AD) whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable.

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AD Pipeline Watch: Apogee’s APG777 Continues to Shine in Phase 1 AD Study

The Dermatology Digest

APG777 continues to show promise in atopic dermatitis (AD), according to early data. APG777, in single doses up to 1,200mg or multiple doses of 300mg, showed a well-tolerated safety profile. Apogee Therapeutics, Inc. The company expects to report 16-week topline data from Part A of the trial in the second half of 2025.