Clinical trial

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of Valbenazine for the Treatment of Chorea Associated With Huntington Disease

Name
NBI-98854-HD3005
Description
This is a Phase 3, randomized, double-blind, placebo-controlled study to evaluate the efficacy, safety, and tolerability of valbenazine to treat chorea in participants with Huntington disease.
Trial arms
Trial start
2019-11-13
Estimated PCD
2021-10-15
Trial end
2021-10-26
Status
Completed
Phase
Early phase I
Treatment
Valbenazine
vesicular monoamine transporter 2 (VMAT2) inhibitor
Arms:
Valbenazine
Other names:
NBI-98854
Placebo
non-active dosage form
Arms:
Placebo
Size
128
Primary endpoint
Change From Screening Period Baseline to Maintenance Period in the Unified Huntington's Disease Rating Scale (UHDRS) Total Maximal Chorea (TMC) Score.
Baseline (average of screening and Day -1), maintenance (average of Weeks 10 and 12)
Eligibility criteria
Inclusion Criteria: 1. Have a clinical diagnosis of Huntington Disease (HD) with chorea 2. Be able to walk, with or without the assistance of a person or device 3. Participants of childbearing potential who do not practice total abstinence must agree to use hormonal or two forms of nonhormonal contraception (dual contraception) consistently while participating in the study until 30 days (females) or 90 days (males) after the last dose of the study drug 4. Be able to read and understand English Exclusion Criteria: 1. Have a history of previously established therapy with a VMAT2 inhibitor, in the judgement of the investigator 2. Have difficulty swallowing 3. Are currently pregnant or breastfeeding 4. Have a known history of long QT syndrome, cardiac tachyarrhythmia, left bundle-branch block, atrioventricular block, uncontrolled bradyarrhythmia, or heart failure 5. Have an unstable or serious medical or psychiatric illness 6. Have a significant risk of suicidal behavior 7. Have a history of substance dependence or substance (drug) or alcohol abuse, within 1 year of screening 8. If taking antidepressant therapy, be on a stable regimen 9. Have received gene therapy at any time 10. Have received an investigational drug in a clinical study within 30 days of the baseline visit or plan to use such investigational drug (other than valbenazine) during the study 11. Have had a blood loss ≥550 milliliters (mL) or donated blood within 30 days before the baseline visit 12. Had a medically significant illness within 30 days before baseline, or any history of neuroleptic malignant syndrome
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 128, 'type': 'ACTUAL'}}
Updated at
2023-10-11

1 organization

2 products

2 indications

Indication
Chorea
Product
Placebo