SICCA Participant Enrollment is closed.
We are accepting applications for clinical data and/or specimen requests from the SICCA Biorepository.
The current cycle of applications are due February 1, 2014. Click the button below for further information:
Coming Soon in early 2014: New SICCA Website! Explore clinical data and run basic statistics, view list of available specimens and apply online.
Stay tuned for details!
SICCA is dedicated to the well-being of individuals with Sjögren's Syndrome.
The Sjögren's Syndrome International Collaborative Clinical Alliance (SICCA) comprises a group of clinical and laboratory investigators from across the world who focus on the development of the International Sjögren's Syndrome Registry.
The International Sjögren's Syndrome Registry has the goal of promoting cutting-edge research in the area of Sjögren's syndrome with emphasis on diagnosis, epidemiology, causes, prevention and treatment.
The International Sjögren's Syndrome 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 (Agency Award #N01DE32636).
Please explore the site for more information about SICCA.
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The contents of this website are regularly updated. This page was last updated November 14, 2013.
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