This is a global, phase 3, randomized, double-blind, parallel-group, 2-arm, placebo controlled, multicenter trial designed to compare the efficacy, safety and tolerability of a fixed dose of SEP-363856 (75 millligrams per day \[mg/day\]) to placebo over an 8-week double-blind treatment period in adults with generalized anxiety disorder (GAD).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
384
Oral tablet
Oral tablet
Anderson Clinical Research
Redlands, California, United States
RECRUITINGClinical Neuroscience Solutions Inc. (CNS) - Orlando
Orlando, Florida, United States
RECRUITINGLumina Clinical Research Center
Cherry Hill, New Jersey, United States
Change From Baseline at Week 8 in Hamilton Anxiety Rating Scale (HAM-A) Total Score
The HAM-A is a clinician-administered rating scale developed to quantify the severity of anxiety symptomatology. It consists of 14 items, each defined by a series of symptoms. Each item is scored on a 5-point Likert-type scale ranging from 0 (absent) to 4 (very severe). The total score ranges from 0 to 56, with higher scores indicating greater severity.
Time frame: Baseline, Week 8
Change From Baseline at Week 8 in Clinical Global Impression-Severity (CGI-S) Score
The CGI-S is a clinician-rated assessment of the participant's current illness state on a 7-point Likert-type scale (1=normal, not at all ill; 7=among the most extremely ill patients), where a higher score is associated with greater illness severity. A decrease in value indicates improvement.
Time frame: Baseline, Week 8
Proportion of Participants Achieving HAM-A Response Criterion at Week 8 (Greater Than or Equal to [≥] 50 Percent [%] Improvement From Baseline in HAM-A Total Score)
Time frame: Baseline, Week 8
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Basil Clinical
Jamaica, New York, United States
RECRUITINGCore Clinical Research
Everett, Washington, United States
RECRUITING