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                <identifier>oai:data.mendeley.com/xbn5k9fgff.1</identifier>
                <datestamp>2021-02-11T13:57:56Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Ellinwood, Amy</dc:creator>
    <dc:title>Baricitinib in patients with moderate-to-severe atopic dermatitis:  Results from a randomized monotherapy Phase 3 trial in the United States and Canada (BREEZE-AD5) - Supplement</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Background: Baricitinib, an oral, selective Janus kinase (JAK)1/JAK2 inhibitor, is being studied for moderate-to-severe atopic dermatitis (AD) in adults.	

Objective: To evaluate the efficacy and safety of baricitinib monotherapy in a North American Phase 3 trial (BREEZE-AD5/NCT03435081) of adults with moderate-to-severe AD who responded inadequately or were intolerant to topical therapy.

Methods: Patients (N=440) were randomized 1:1:1 to once-daily placebo or baricitinib (1 mg or 2 mg). The primary endpoint was the proportion of patients achieving ≥75% reduction in the Eczema Area and Severity Index (EASI75) at Week 16. A key secondary endpoint was the proportion of patients achieving a validated Investigator Global Assessment for AD (vIGA-AD™) score of 0 (clear)/1(almost clear) with ≥2-point improvement.

Results: At Week 16, the proportion of patients achieving EASI75 was 8%, 13%, and 30% (P &lt;.001, 2 mg vs. placebo) and those with a vIGA-AD 0/1 were 5%, 13%, and 24% (P &lt;.001, 2 mg vs. placebo), for placebo, baricitinib 1 mg, and 2 mg, respectively. Safety findings were similar to other baricitinib AD studies.

Limitations: Short-term clinical trial results may not be generalizable to real-world settings.

Conclusion: Baricitinib was efficacious for patients with moderate-to-severe AD with no new safety findings over 16 weeks.  </dc:description>
    <dc:subject>Atopic Dermatitis</dc:subject>
    <dc:contributor>Simpson, Eric</dc:contributor>
    <dc:contributor>Forman, Seth</dc:contributor>
    <dc:contributor>Silverberg, Jonathan</dc:contributor>
    <dc:contributor>Zirwas, Matthew</dc:contributor>
    <dc:contributor>Maverakis, Emanual</dc:contributor>
    <dc:contributor>Han, George</dc:contributor>
    <dc:contributor>Guttman-Yassky, Emma</dc:contributor>
    <dc:contributor>Marnell, Daniel</dc:contributor>
    <dc:contributor>Bissonnette, Robert</dc:contributor>
    <dc:contributor>Waibel, Jill</dc:contributor>
    <dc:contributor>Nunes, Fabio</dc:contributor>
    <dc:contributor>DeLozier, Amy</dc:contributor>
    <dc:contributor>Angle, Robinette</dc:contributor>
    <dc:contributor>Gamalo, Margaret</dc:contributor>
    <dc:contributor>Holzwarth, Katrin</dc:contributor>
    <dc:contributor>Goldblum, Orin</dc:contributor>
    <dc:contributor>Zhong, Jinglin</dc:contributor>
    <dc:contributor>Janes, Jonathan</dc:contributor>
    <dc:contributor>Papp, Kim</dc:contributor>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/xbn5k9fgff.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/xbn5k9fgff.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/xbn5k9fgff</dc:relation>
    <dc:date>2021-02-11T13:57:56Z</dc:date>
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