Nail Psoriasis Does Not Affect Skin Response to Ixekizumab in Patients With Moderate-To-Severe Psoriasis

August 2020 | Volume 19 | Issue 8 | Original Article | 741 | Copyright © August 2020


Published online July 24, 2020

Phoebe Rich MD,a Orin Goldblum MD,b Damon Disch PhD,b Chen-Yen Lin PhD,b Joseph F. Merola MD,c Boni Elewski MDd

aOregon Health and Science University’s Center for Health and Healing, Portland, OR bEli Lilly and Company, Indianapolis, IN cBrigham and Women's Hospital, Harvard Medical School, Boston, MA dUniversity of Alabama at Birmingham, Birmingham, AL

of the nail plate. Optimal effect may take up to or exceed 52 weeks of therapy.16 In UNCOVER-3, continued improvement of fingernail psoriasis was seen in patients treated with ixekizumab through 60 weeks.12,14 Long-term efficacy and safety of ixekizumab for treatment of moderate-to-severe plaque psoriasis has been reported to 108 weeks.17 Taken together, ixekizumab demonstrated early efficacy in fingernail psoriasis within 12 weeks and continued efficacy in open-label treatment to 60 weeks.

In conclusion, this study demonstrated that patients both with and without nail psoriasis responded well to ixekizumab. In contrast to previous reports in which the presence of nail psoriasis was a negative prognostic factor for psoriasis,8,9 the presence of nail psoriasis did not negatively affect skin response in patients treated with ixekizumab.

DISCLOSURES

Dr. Rich has received research and educational grants from AbbVie, Allergan, Anacor Pharmaceuticals, Boehringer Ingelheim, Cassiopea SpA, Dermira, Eli Lilly and Company, Galderma Laboratories LP, Janssen Ortho Inc., Kadmon Corporation, Leo Pharma, Merck, Moberg Derma, Novartis, Pfizer, Ranbaxy Laboratories Limited, Sandoz, Viamet Pharmaceutical Inc., Innovation Pharmaceuticals (Cellceutix), and Cutanea Life Sciences. Dr. Merola is a consultant and/or investigator for Merck Research Laboratories, AbbVie, Dermavant Sciences Ltd., Eli Lilly and Company, Novartis, Janssen, UCB, Samumed LLC, Celgene, Sanofi Regeneron, GlaxoSmithKline, Almirall, Sun Pharma, Biogen, Pfizer, Incyte, Aclaris Therapeutics, EMD Serono and Leo Pharma. Dr. Elewski has received research and support from AbbVie, AnaptysBio, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, Incycte, Leo Pharma, Eli Lilly and Company, Merck, Menlo Therapeutics, Novartis, Pfizer, Regeneron Pharmaceuticals, Sun Pharma, Bausch Health (Valeant Pharmaceuticals), and Vanda Pharmaceuticals and is a consultant for Boehringer Ingelheim, Celgene, Leo Pharma, Eli Lilly and Company, and Menlo Therapeutics. Dr. Goldblum and Dr. Lin own stock in and are employees of Eli Lilly and Company. Dr. Disch is an Eli Lilly and Company retiree and owns stock in Lilly and other pharmaceutical companies under the independent management of a financial advisor.

ACKNOWLEDGMENTS

This study was sponsored by Eli Lilly and Company. The authors would like to thank the patients and the investigators who participated in these studies. Medical writing services was provided by Sarah Beckman, PhD, and editorial support was provided by Noelle Gasco of Syneos Health, which were funded by Eli Lilly and Company.

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AUTHOR CORRESPONDENCE

Orin Goldblum MD goldblum_orin_m@lilly.com