The main objective of this study is to evaluate the efficacy, safety, and tolerability of NBI-827104 in adults with essential tremor.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
31
Capsules for oral administration
Capsules matching NBI-827104 for oral administration
Neurocrine Clinical Site
Leiden, CL, Netherlands
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
Change from Baseline in Essential Tremor Rating Assessment Scale (TETRAS) Performance Score
Time frame: Baseline up to Day 28 of each treatment period
Change from Baseline in TETRAS Activities of Daily Living (ADL) Score
Time frame: Baseline up to Day 28 of each treatment period
Clinical Global Impression of Change (CGI-C)
Time frame: Up to Day 28 of each treatment period
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