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Completed

NCT Number: NCT02674321

A Pilot Study Of SD-809 (Deutetrabenazine) In Moderate To Severe Tourette Syndrome (TS)

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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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 12 to 18 years of age, inclusive, at Screening.
  • Patient has a Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) diagnosis of Tourette Syndrome and has manifested motor and phonic tics within 3 months before the Screening visit
  • Patient has total tic score of ≥19 on the YGTSS
  • Tic severity and frequency has been stable for at least 2 weeks before the Screening visit
  • Willing to adhere to medication regimen and to comply with all procedures
  • Patient is in good general health, as indicated by medical and psychiatric history and physical examination
  • Patient and parent/guardian have provided written, informed consent (and written assent, as appropriate)
  • Female patients of childbearing potential agree to use an acceptable method of contraception
  • Additional criteria apply, please contact the investigator for more information

Exclusion criteria

  • Patient has a serious untreated or undertreated psychiatric illness
  • Patient has a history of suicidal ideation or behavior
  • Patient has received tetrabenazine, neuroleptics, benzodiazepines, topiramate, dopamine receptor antagonists within 14 days of Screening or Baseline; or botulinum toxin within 3 months of Screening or Baseline
  • Patient is being treated with deep brain stimulation for control of tics
  • Patient has a progressive or degenerative neurological disorder or a structural disorder of the brain
  • Patient has participated in an investigational drug or device trial within 30 days of Screening
  • Patient is pregnant or breastfeeding at Screening or Baseline
  • Patient has a history of alcohol or substance abuse in the previous 12 months, as defined in the DSM-V
  • Additional criteria apply, please contact the investigator for more information

Treatment and study plan

SD-809

Drug

Primary outcomes

  1. Safety

    Time frame: 8 weeks

    Incidence of adverse events (AEs), serious AEs, severe AEs, drug related AEs, AEs leading to withdrawal.

Secondary outcomes

  1. Change from Baseline in Total Tic Score of the Yale Global Tic Severity Scale (YGTSS)

    Time frame: Baseline, Weeks 2, 4 and 8

  2. Change from Baseline in Impairment Score of the Yale Global Tic Severity Scale (YGTSS)

    Time frame: Baseline, Weeks 2, 4, and 8

  3. Change from Baseline in Global Severity Score of the Yale Global Tic Severity Scale (YGTSS)

    Time frame: Baseline, Weeks 2, 4, and 8

  4. Change from Baseline in Tourette Syndrome Clinical Global Impression

    Time frame: Baseline, Weeks 2, 4, and 8

  5. Patient Global Impression of Change (TS-PGIC)

    Time frame: Weeks 2, 4, and 8

Other outcomes

  1. Pharmacokinetic parameters

    Time frame: 8 weeks

Sponsors and collaborators

Lead sponsor

Auspex Pharmaceuticals, Inc.

Industry

Registry information

Official study title

A Pilot Study Of SD-809 (Deutetrabenazine) In Moderate To Severe Tourette Syndrome

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Feb 4, 2016
Registry last updated
Nov 9, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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