SICCA is dedicated to the well-being of individuals with Sjögren's Syndrome.

The Sjogren's International Collaborative Clinical Alliance (SICCA) comprises a group of clinical and laboratory investigators from around the world who have developed the International Sjögren's Syndrome Biorepository and Data Registry.

The International Sjögren's Syndrome Biorepository and Data Registry has the goal of promoting high-quality, cutting-edge research in the area of Sjögren's syndrome with emphasis on diagnosis, epidemiology, causes, prevention and treatment.

The International Sjögren's Syndrome Biorepository and Data Registry is funded by the US Public Health Service/National Institutes of Health (NIH) National Institute of Dental and Craniofacial Research (NIDCR), the National Eye Institute (NEI), and the National Institutes of Health Office for Research on Women's Health, Bethesda, MD, USA (contract #HHSN268201300057C).

Please explore the site for more information about SICCA.