-
A Phase III Open-Label, Outpatient Extension
Study to Assess the Long-Term Safety and Efficacy of Two Dose
Levels of a Modified Release Formulation of Study Drug in Adult
Primary Insomnia Patients with Sleep Maintenance Difficulties
-
Multi-Center, Randomized, Double-Blind, Parallel-Group,
Placebo-Controlled, Fixed-Dose Study Evaluating the Efficacy,
Safety and Tolerability of Two Doses of a Once-Daily Oral Formulation
of Study Drug in Subjects with Major Depressive Disorder for
a Treatment Period of Eight Weeks
-
Analysis of Survey Data and Validation of the
Original Dementia Progression Scale
-
An Open-Label Extension Study to Assess the
Long-Term Safety and Tolerability of Study Drug in the Treatment
of Mild Cognitive Impairment
-
Study Drug Versus Study Drug in the Treatment
of Major Depressive Disorder
-
A Multi-Center, Double-Blind, Placebo-Controlled,
Randomized Parallel Group Evaluation of the Efficacy of a Flexible
Dose of Study Drug versus Placebo as Add-On Therapy in Schizoprhenia
-
A Randomized, Open Label, Long Term, Multi Center
Study of the Safety of Study Drug (for Alcohol and/or Opiate
Dependence)
-
An Open-Label Study of Tolerability, Clinical
Response, and Satisfaction in Adult Bipolar I Subjects Optimizing
Initiation of Therapy Using Administration of Study Precautions
and Study Drug Titration Packs
-
A Randomized Double-Blind Study of Study Drug
Versus Study Drug in the Treatment of Schizophrenia
-
A Dose-Ranging Placebo-Controlled Study of Study
Drug at the doses of 0.5 mg, 2 mg, and 8 mg for 12 Weeks in
Patients with Mild-to-Moderate Alzheimer’s Disease