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COMPLETED
NCT06267846
PHASE2

A Study to Evaluate the Efficacy and Safety of NBI-1070770 in Adults With Major Depressive Disorder

Sponsor: Neurocrine Biosciences

View on ClinicalTrials.gov

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

Interventions

DRUG

NBI-1070770

Suspension for oral administration

DRUG

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