A Study of Buntanetap in Participants With PD
Sponsored by Annovis Bio Inc.
About this study
This study will examine the long-term safety of buntanetap in participants with PD. This will be a 36-month open-label safety study. This study will be conducted with two cohorts. Cohort 1 will enroll via invitation only for PD participants who have previously participated in buntanetap clinical trials. Cohort 2 will be for PD participants who are receiving deep brain stimulation (DBS) treatment. Qualified participants will receive buntanetap 30mg QD after a screening period of up to 42 days.
Enrolling at this location
Medical University of South Carolina (MUSC) - The Murray Center for Research on Parkinson's Disease
Charleston, South Carolina
I'm interestedThis study also enrolls at 26 other locations. See all.
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Trial data sourced from ClinicalTrials.gov.