Teva Investigational Site #101
Houston, Texas, 77030, United States
NCT Number: NCT02674321
The purpose of this study is to evaluate safety, tolerability and preliminary efficacy of SD-809 in the treatment of motor and phonic tics of Tourette Syndrome and to evaluate the pharmacokinetic of SD-809 and its metabolites.
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Notify Me12 year–18 year
All sexes
Interventional
Phase 1
Houston, Texas, 77030, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 8 weeks
Incidence of adverse events (AEs), serious AEs, severe AEs, drug related AEs, AEs leading to withdrawal.
Time frame: Baseline, Weeks 2, 4 and 8
Time frame: Baseline, Weeks 2, 4, and 8
Time frame: Baseline, Weeks 2, 4, and 8
Time frame: Baseline, Weeks 2, 4, and 8
Time frame: Weeks 2, 4, and 8
Time frame: 8 weeks
Auspex Pharmaceuticals, Inc.
Industry
A Pilot Study Of SD-809 (Deutetrabenazine) In Moderate To Severe Tourette Syndrome
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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