Safety and Tolerability Study of NBI-98854 for the Treatment of Subjects With Tourette Syndrome

Tourette Syndrome Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02879578
• Other study ID #: NBI-98854-1601
• Status: Completed
• Phase: Phase 2
• Start date: July 25, 2016
• Est. completion date: November 1, 2017

Study information

• Verified date: April 2021
• Source: Neurocrine Biosciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Phase 2, open-label, fixed-dose titration study to evaluate the safety and tolerability of NBI-98854 administered once daily for a total of 24 weeks in children, adolescents, and adults with Tourette Syndrome (TS).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 155
• Est. completion date: November 1, 2017
• Est. primary completion date: November 1, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Years to 64 Years

Eligibility

Inclusion Criteria:

• Have participated in and completed the NBI-98854-1501 (T-Force Green) or NBI-98854-1505 (T-Forward) Phase 2 study

• Have a clinical diagnosis of Tourette Syndrome (TS)

• If using maintenance medication(s) for TS or TS spectrum diagnoses (e.g. obsessive-compulsive disorder [OCD], Attention-Deficit Hyperactivity Disorder [ADHD]), be on stable doses

• Subjects of childbearing potential who do not practice total abstinence must agree to use hormonal or two forms of nonhormonal contraception (dual contraception) consistently during the screening, treatment and follow-up periods of the study

• Adolescent and adult subjects (12 to 64 years of age) must have a negative urine drug screen for amphetamines, barbiturates, benzodiazepine, phencyclidine, cocaine, opiates, or cannabinoids and a negative alcohol screen. Subjects who are on stable doses of prescribed and supervised (not as needed) benzodiazepines, opiates, or psychostimulants (for subjects with comorbid ADHD) are allowed to participate in the study

• Be in good general health

Exclusion Criteria:

• Have an active, clinically significant unstable medical condition within 1 month prior to screening

• Have a known history of long QT syndrome or cardiac arrhythmia

• Have a known history of neuroleptic malignant syndrome

• Have a cancer diagnosis within 3 years prior to screening (some exceptions allowed)

• Have a blood loss =250 mL or donated blood within 56 days prior to screening (subjects 6 to 17 years of age); have a blood loss =550 mL or donated blood within 30 days prior to screening (subjects 18 to 64 years of age)

• Have a known history of substance dependence, substance (drug) or alcohol abuse

• Have a significant risk of suicidal or violent behavior

• Have initiated Comprehensive Behavioral Intervention for Tics (CBIT) during the screening period or at baseline or plan to initiate CBIT during the study

• Have received an investigational drug within 30 days before screening or plan to use an investigational drug (other than NBI-98854) during the study

Related Conditions & MeSH terms

• Syndrome
• Tourette Syndrome

Intervention

Drug:
• Valbenazine

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Neurocrine Biosciences

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Frequency of Treatment-emergent Adverse Events (TEAEs)	A TEAE is an adverse event not present prior to the initiation of study drug dosing, or is an already present event that worsens either in intensity or frequency following the initiation of study drug dosing.	Baseline through Week 28