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Completed

NCT Number: NCT04880616

Safety, Efficacy, and Tolerability of NBI-827104 for the Treatment of Essential Tremor

The main objective of this study is to evaluate the efficacy, safety, and tolerability of NBI-827104 in adults with essential tremor.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Neurocrine Clinical Site

Leiden, CL, 2333, Netherlands

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male or female subjects, 18 to 75 years of age, inclusive at screening.
  • Body mass index (BMI) between 18 and 35 kg/m², inclusive, at screening.
  • Diagnosis of Essential Tremor (inclusive of Essential Tremor plus) as defined by the Movement Disorders Society Consensus Criteria for Tremor.
  • Confirmation of bilateral upper limb action tremor in the absence of overt dystonia, ataxia, or parkinsonism.
  • History of onset of tremor before 65 years of age.
  • Tremor Performance score of ≥ 2 on at least 2 of the 6 upper limb manoeuvres (Item 4) on the TETRAS Performance Subscale and a total TETRAS Performance score ≥15 at screening.
  • All women of childbearing potential and all males must practice effective contraception during the study and be willing and able to continue contraception for at least 90 days after their last dose of study drug.

Exclusion criteria

  • Evidence of any acute (at screening or prior to first dose) or chronic disease or condition that could interfere with, or for which the treatment might interfere with, the conduct of the study, or that would pose an unacceptable risk to the subject in the opinion of the investigator.
  • Have direct or indirect trauma to the nervous system within 3 months preceding the onset of tremor.
  • Have known history of other medical or neurological conditions that may cause or explain subject's tremor.
  • Have had prior magnetic resonance guided focused ultrasound or surgical intervention (e.g., deep brain stimulation, ablative thalamotomy or gamma knife thalamotomy).
  • Have a history or evidence of clinically significant cardiac conduction abnormality, uncontrolled bradyarrhythmia, heart failure, or long QT syndrome.

Treatment and study plan

NBI-827104

Drug

Capsules for oral administration

Placebo

Drug

Capsules matching NBI-827104 for oral administration

Primary outcomes

  1. Change from Baseline to Day 28 of Each Treatment Period in Amplitude at Peak Frequency of Postural Tremor

    Time frame: Baseline and Day 28 of each treatment period

Secondary outcomes

  1. Change from Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Score

    Time frame: Baseline up to Day 28 of each treatment period

  2. Change from Baseline in TETRAS Activities of Daily Living (ADL) Score

    Time frame: Baseline up to Day 28 of each treatment period

  3. Clinical Global Impression of Change (CGI-C)

    Time frame: Up to Day 28 of each treatment period

Sponsors and collaborators

Lead sponsor

Neurocrine Biosciences

Industry

Registry information

Official study title

A Phase 2 Randomized, Double-Blind, Placebo-Controlled, Crossover Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of NBI-827104 in Subjects With Essential Tremor

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
May 11, 2021
Registry last updated
Jul 12, 2022

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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