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A Study to Evaluate the Efficacy and Safety of NBI-1070770 in Adults With Major Depressive Disorder
Sponsor: Neurocrine Biosciences
Summary
To evaluate the efficacy, safety, and tolerability of NBI-1070770 compared to placebo on improving symptoms of depression in participants with major depressive disorder (MDD).
Official title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Efficacy, Safety, and Tolerability of NBI-1070770 in Adults With Major Depressive Disorder
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
73
Start Date
2024-03-20
Completion Date
2025-09-11
Last Updated
2026-07-17
Healthy Volunteers
No
Conditions
Interventions
NBI-1070770
Suspension for oral administration
Placebo
Suspension for oral administration
Locations (13)
Neurocrine Clinical Site
Little Rock, Arkansas, United States
Neurocrine Clinical Site
Rogers, Arkansas, United States
Neurocrine Clinical Site
Lemon Grove, California, United States
Neurocrine Clinical Site
Long Beach, California, United States
Neurocrine Clinical Site
Hollywood, Florida, United States
Neurocrine Clinical Site
Maitland, Florida, United States
Neurocrine Clinical Site
Decatur, Georgia, United States
Neurocrine Clinical Site
Savannah, Georgia, United States
Neurocrine Clinical Site
Gaithersburg, Maryland, United States
Neurocrine Clinical Site
Dayton, Ohio, United States
Neurocrine Clinical Site
North Canton, Ohio, United States
Neurocrine Clinical Site
Houston, Texas, United States
Neurocrine Clinical Site
Richardson, Texas, United States