Recent advances in the search for a targeted immunomodulatory therapy for primary Sjögren's syndrome [version 1; peer review: 2 approved]
Primary Sjögren's syndrome is a chronic autoimmune disease characterized by salivary and lacrimal gland dysfunction, leading to substantial morbidity and reduced quality of life. Many patients with primary Sjögren's syndrome also have extraglandular systemic complications, some of which ca...
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Published in | F1000 research Vol. 8; p. 1532 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
Faculty of 1000 Ltd
2019
F1000 Research Limited F1000 Research Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | Primary Sjögren's syndrome is a chronic autoimmune disease characterized by salivary and lacrimal gland dysfunction, leading to substantial morbidity and reduced quality of life. Many patients with primary Sjögren's syndrome also have extraglandular systemic complications, some of which can be organ- or life-threatening. Over the last decade, numerous targeted immunomodulatory therapies for primary Sjögren's syndrome have failed to show a benefit in clinical trials, and as yet no disease-modifying therapy has been approved for this disease. Herein, we provide an updated review of the clinical trial landscape for primary Sjögren's syndrome and the numerous efforts to move the field forward, including the development of new classification criteria and outcome measures, the results of recent clinical trials in this field, the challenges faced in the search for effective therapies, and the expanding pipeline of novel therapies under development. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Competing interests: DLL declares that he has no competing interests. EWS has been a consultant for and received a research grant from Bristol-Myers Squibb and has been a consultant for Viela Bio and Abbvie. |
ISSN: | 2046-1402 2046-1402 |
DOI: | 10.12688/f1000research.19842.1 |