A 24‐Week, Phase IIa, Randomized, Double‐Blind, Placebo‐Controlled Study of Ziritaxestat in Early Diffuse Cutaneous Systemic Sclerosis

Author:

Khanna Dinesh1ORCID,Denton Christopher P.2ORCID,Furst Daniel E.3ORCID,Mayes Maureen D.4ORCID,Matucci‐Cerinic Marco5,Smith Vanessa6,de Vries Dick7,Ford Paul8,Bauer Yasmina9,Randall Matthew J.9,Ebrahimpoor Mitra7,Kupcsik Laszlo8,Stiers Pieter‐Jan8,Deberdt Liesbeth8,Prasad Niyati8,Lim Sharlene10,Pujuguet Philippe11,Ahmed Sohail9

Affiliation:

1. University of Michigan Scleroderma Program Ann Arbor Michigan

2. Royal Free Hospital, University College London London UK

3. David Geffen School of Medicine at UCLA, Los Angeles, California, University of Washington, Seattle, Washington, and University of Florence Florence Italy

4. University of Texas Health Science Center at Houston

5. Unit of Immunology, Rheumatology, Allergy and Rare Diseases (UnIRAR), IRCCS San Raffaele Hospital, Milan, Italy, Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy, and Division of Rheumatology, AOUC Florence Italy

6. Department of Internal Medicine, Ghent University, Ghent, Belgium, and Department of Rheumatology, Ghent University Hospital, Ghent, Belgium, and Unit for Molecular Immunology and Inflammation, VIB Inflammation Research Center (IRC) Ghent Belgium

7. Galapagos BV Leiden Netherlands

8. Galapagos NV Mechelen Belgium

9. Galapagos GmbH Basel Switzerland

10. Gilead Sciences, Inc. Foster City California

11. Galapagos SASU Romainville France

Abstract

ObjectiveWe undertook this study to explore the efficacy, safety, and tolerability of ziritaxestat, a selective autotaxin inhibitor, in patients with early diffuse cutaneous systemic sclerosis (dcSSc).MethodsNOVESA was a 24‐week, multicenter, phase IIa, double‐blind, placebo‐controlled study. Adults with dcSSc were randomized to oral ziritaxestat 600 mg once daily or matching placebo. The primary efficacy end point was change from baseline in modified Rodnan skin score (MRSS) at week 24. Secondary end points assessed safety and tolerability; other end points included assessment of skin and blood biomarkers. Patients in NOVESA could enter a 104‐week open‐label extension (OLE).ResultsPatients were randomized to ziritaxestat (n = 21) or placebo (n = 12). Reduction in MRSS was significantly greater in the ziritaxestat group versus the placebo group (–8.9 versus –6.0 units, respectively; P = 0.0411). Placebo patients switching to ziritaxestat in the OLE showed similar reductions in MRSS to those observed for ziritaxestat patients in the parent study. Ziritaxestat was well tolerated; the most frequent treatment‐related treatment‐emergent adverse events were headache and diarrhea. Circulating lysophosphatidic acid (LPA) C18:2 was significantly reduced, demonstrating ziritaxestat target engagement, and levels of fibrosis biomarkers were reduced in the blood. No differentially expressed genes were identified in skin biopsies. Significant changes in 109 genes were identified in blood samples.ConclusionZiritaxestat resulted in significantly greater reduction in MRSS at week 24 than placebo; no new safety signals emerged. Biomarker analysis suggests ziritaxestat may reduce fibrosis. Modulation of the autotaxin/LPA pathway could improve skin involvement in patients with dcSSc. A plain language summary is provided in the Supplementary Material, available on the Arthritis & Rheumatology website at https://onlinelibrary.wiley.com/doi/10.1002/art.42477.image

Funder

Galapagos NV

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Recent Advances in Treatment of Systemic Sclerosis and Morphea;American Journal of Clinical Dermatology;2023-12-12

2. Biomarkers in the Pathogenesis, Diagnosis, and Treatment of Systemic Sclerosis;Journal of Inflammation Research;2023-10

3. Biomarkers in Systemic Sclerosis: An Overview;Current Issues in Molecular Biology;2023-09-25

4. Clinical Trials in Systemic Sclerosis: Crossroads and Opportunities;Arthritis & Rheumatology;2023-06-23

5. Role of autotaxin in systemic lupus erythematosus;Frontiers in Medicine;2023-04-04

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