Characterizing real world safety profile of oral Janus kinase inhibitors among adult atopic dermatitis patients: evidence transporting from the rheumatoid arthritis population

Author:

Montez-Rath Maria E.1,Lubwama Robert2,Kapphahn Kris3,Ling Albee Y.3,LoCasale Robert2,Robinson Lacey2,Chandross Karen J.24,Desai Manisha3

Affiliation:

1. Department of Medicine, Division of Nephrology, Stanford University School of Medicine, Palo Alto, CA, USA

2. Sanofi, Bridgewater, NJ, USA

3. Department of Medicine, Division of Biomedical Informatics Research, Quantitative Sciences Unit, Stanford University School of Medicine, Palo Alto, CA, USA

4. Sanofi, R&D, Bridgewater, NJ, USA

Publisher

Informa UK Limited

Subject

General Medicine

Reference34 articles.

1. Atopic Dermatitis in America Study: A Cross-Sectional Study Examining the Prevalence and Disease Burden of Atopic Dermatitis in the US Adult Population

2. 204 A real-world study evaluating adeQUacy of Existing Systemic Treatments for patients with moderate-to-severe Atopic Dermatitis (AD-QUEST): Baseline treatment patterns and unmet needs assessment

3. The rheumatoid arthritis patient in the clinic: comparing more than 1300 consecutive DMARD courses

4.

JAK Inhibitors in Rheumatoid Arthritis: An Evidence-Based Review on the Emerging Clinical Data

5. AbbVie. European Commission Approves RINVOQ (upadacitinib) as First JAK inhibitor in the European Union for the treatment of both adults and adolescents with moderate to severe atopic dermatitis [Internet]; 2021 [cited 2021 Aug 24]. Available from: https://www.prnewswire.com/news-releases/european-commission-approves-rinvoq-upadacitinib-as-first-jak-inhibitor-in-the-european-union-for-the-treatment-of-both-adults-and-adolescents-with-moderate-to-severe-atopic-dermatitis-301361058.html.

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