Publications by authors named "Mark Levenberg"

Introduction: Early prediction of abrocitinib efficacy in atopic dermatitis (AD) could help identify candidates for an early dose increase. A predictive model determined week 12 efficacy based on week 4 responses in patients receiving abrocitinib 100 mg/day and assessed the effect of an abrocitinib dose increase on platelet counts.

Methods: Analysis included the phase 3 trials JADE MONO-1 (NCT03349060), MONO-2 (NCT03575871), COMPARE (NCT03720470), and TEEN (NCT03796676).

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Article Synopsis
  • The study investigated the effectiveness and safety of the medication abrocitinib for treating moderate-to-severe atopic dermatitis, focusing on different racial and ethnic groups.
  • Data from three trials included self-reported race and ethnicity, as well as Fitzpatrick skin type, to compare responses to the treatment.
  • Results showed that abrocitinib significantly improved skin conditions for all racial groups, with the most pronounced effects in White patients; however, Black patients had similar responses to both doses tested and reported more treatment-related side effects compared to Asian patients.
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Introduction: For many, atopic dermatitis (AD) is not adequately controlled with topical regimens. This analysis examined treatment using advanced therapies and associated costs.

Methods: The IQVIA Health Plan Claims data set was analyzed.

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Background: Atopic dermatitis is a chronic inflammatory skin disease that affects up to 13% of children and 10% of adults in the United States. Among patients and their families, atopic dermatitis has a considerable effect on quality of life and represents a substantial economic burden.

Objective: To describe the impact and challenges of atopic dermatitis and to provide nondermatologists in the healthcare community an enhanced understanding of atopic dermatitis to facilitate treatment and pharmacy benefit discussions.

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Article Synopsis
  • Atopic dermatitis (AD) is a common skin condition treated with topical corticosteroids (TCS) and calcineurin inhibitors (TCI), and crisaborole is a newly approved non-steroidal treatment for mild-to-moderate cases.
  • The study assesses the real-world use and costs of TCS and TCI, as well as the budget impact of introducing crisaborole over two years for health insurance providers.
  • Results showed that while the budget impact of crisaborole was relatively modest—a cost increase of $350,946 for TCS/TCI patients—its adoption could lower costs for patients using TCIs by about $22,871.
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