The primary purpose of this study is to determine the safety and efficacy of oral RG2417 (Uridine) when administered to patients with Bipolar I depression twice daily for six weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
80
Stanford University
Stanford, California, United States
Carman Research
Smyrna, Georgia, United States
Indiana University-Purdue University Indianapolis
Indianapolis, Indiana, United States
Improvement of MADRS and CGI BP C for RG2417 treatment in comparison to placebo
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Marc Hertzman, MD, PC
Rockville, Maryland, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
Medical & Behavioral Health Research, PC
New York, New York, United States
University of Cincinnati
Cincinnati, Ohio, United States
Cleveland Clinic Foundation
Cleveland, Ohio, United States
Future Search Trials of Austin
Austin, Texas, United States
Future Search Trials of Dallas
Dallas, Texas, United States
...and 1 more locations