This study will be conducted to evaluate the efficacy, safety, and tolerability of AVP-786, as compared with placebo, for the treatment of negative symptoms of schizophrenia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
136
Change from Baseline to Week 15 in the Positive and Negative Syndrome Scale (PANSS) Marder Negative Factors Score
Time frame: Baseline; Week 15
Change from Baseline to Week 15 in the Negative Symptom Assessment-16 (NSA-16) Global Negative Symptom Score
Time frame: Baseline; Week 15
Change from Baseline to Week 15 in the Patient Global Impression of Severity (PGI-S) Score
Time frame: Baseline; Week 15
Change from Baseline to Week 15 in the Patient Global Impression of Change (PGI-C) Score
Time frame: Baseline; Week 15
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Clinical Research Site
Little Rock, Arkansas, United States
Clinical Research Site #840-041
Anaheim, California, United States
Clinical Research Site #840-013
Bellflower, California, United States
Clinical Research Site #840-079
Costa Mesa, California, United States
Clinical Research Site #840-027
Culver City, California, United States
Clinical Research Site #840-006
Garden Grove, California, United States
Clinical Research Site #840-026
Glendale, California, United States
Clinical Research Site# 840-067
La Habra, California, United States
Clinical Research Site# 840-083
Lafayette, California, United States
Clinical Research Site 840-002
Lemon Grove, California, United States
...and 62 more locations