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Recruiting NCT07365462

Efficacy, Safety, and Tolerability of NBI-1065890 Versus Placebo in Adults With Tardive Dyskinesia

Phase II Interventional Tardive Dyskinesia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: NBI-1065890, Placebo.
Who it may be relevant to
Registry conditions: Tardive Dyskinesia. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of NBI-1065890 in Adult Participants With Tardive Dyskinesia

Overview

The primary objective of this study is to evaluate the efficacy of NBI-1065890 compared with placebo for the treatment of tardive dyskinesia (TD) in adult participants.

Interventions

  • Drug NBI-1065890
    Oral administration
  • Drug Placebo
    Oral administration

Primary outcome measures

  • Change from Baseline in the Abnormal Involuntary Movement Scale (AIMS) Dyskinesia Total Score at Week 8 Based on the Blinded Central AIMS Video Raters' Assessment [Time frame: Baseline and Week 8]
Secondary outcome measures (1)
  • Percentage of Participants Who Are a Clinical Global Impression - Improvement (CGI-I) Responder 1 at Week 8 [Time frame: Week 8]

Eligibility criteria

Inclusion criteria

  • Medically confirmed diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, or major depressive disorder (MDD) as defined in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) for at least 3 months prior to screening.
  • Medically confirmed diagnosis of neuroleptic-induced TD as defined in the DSM-5 for at least 3 months prior to screening.
  • Moderate or severe TD (AIMS Item 8, severity of abnormal movement overall) as assessed by a blinded, external AIMS video reviewer using a video recording of the participant's AIMS assessment administered at the clinical site by a blinded, certified site AIMS rater. The AIMS dyskinesia total score (sum of Items 1 to 7) must be ≥6 as assessed by the blinded, external AIMS video reviewer.

Exclusion criteria

  • Comorbid parkinsonism (drug-induced or otherwise) or more than a minimal level of extrapyramidal signs/symptoms, as documented by a score on the Modified Simpson-Angus Scale (mSAS) (excluding Items 8 and 10) >6 at screening or Day -1 (baseline) or a score >3 in any one item (excluding Items 8 and 10).
  • Barnes Akathisia Rating Scale (BARS) global clinical assessment score ≥2 at screening or Day -1.
  • Brief Psychiatric Rating Scale (BPRS) total score ≥50 at screening or Day -1.
  • Hospitalized for schizophrenia, schizoaffective disorder, bipolar disorder, or MDD within 6 months of screening.
  • Participant has an unstable medical condition or unstable chronic disease.
  • Any known history of neuroleptic malignant syndrome (NMS).

Note: Other protocol-defined inclusion and exclusion criteria may apply.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

United States · 18 centers
  • Neurocrine Clinical Site — Bryant
  • Neurocrine Clinical Site — Chino
  • Neurocrine Clinical Site — Fountain Valley
  • Neurocrine Clinical Site — Huntington Beach
  • Neurocrine Clinical Site — Long Beach
  • Neurocrine Clinical Site — Temecula
  • Neurocrine Clinical Site — Torrance
  • Neurocrine Clinical Site — Boca Raton
  • … and 10 more centers

Identifiers

NCT: NCT07365462 · NBI-1065890-TD2033 · 2025-524104-30-00

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗