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**BUFY01** is an investigational ophthalmic formulation developed by TRB Chemedica International SA for the treatment of **dry eye disease (DED)**. It is being evaluated in a non-inferiority clinical trial (NCT05865457, BUSTON-01) against SVS20, assessing efficacy on DED signs and symptoms, safety, and tolerability over 3 months of daily use. Participants undergo site visits, examinations, and questionnaires; the trial, not yet recruiting as of the latest data, started planning for June 2025.[1][10]
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