Prospective observational registry for cystinuria patients on Thiola EC therapy

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Prospective observational registry for cystinuria patients on Thiola EC therapy

Brief description of study

The purpose of this research study is to follow patients on Thiola EC for two years and collect cystinuria related treatment information in order to see how they are doing. Thiola EC is Food and Drug Administration (FDA) approved for the treatment of cystinuria. This study is not testing Thiola EC.

Clinical Study Identifier: s20-00331

ClinicalTrials.gov Identifier: NCT05048563

Principal Investigator: David S. Goldfarb.

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