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Completed Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT06267846

Public ClinicalTrials.gov record NCT06267846. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 11, 2026, 9:00 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT06267846
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Neurocrine Biosciences
Industry
Enrollment
73 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 20, 2024 (Actual)
Primary completion
Jul 25, 2025 (Actual)
Completion
Sep 11, 2025 (Actual)
Last update posted
Jul 17, 2026

2024 – 2025

United States locations

U.S. sites
13
U.S. states
7
U.S. cities
13
Facility City State ZIP Site status
Neurocrine Clinical Site Little Rock Arkansas 72211 —
Neurocrine Clinical Site Rogers Arkansas 72758 —
Neurocrine Clinical Site Lemon Grove California 91945 —
Neurocrine Clinical Site Long Beach California 90806 —
Neurocrine Clinical Site Hollywood Florida 33024 —
Neurocrine Clinical Site Maitland Florida 32751 —
Neurocrine Clinical Site Decatur Georgia 30030 —
Neurocrine Clinical Site Savannah Georgia 31405 —
Neurocrine Clinical Site Gaithersburg Maryland 20877 —
Neurocrine Clinical Site Dayton Ohio 45439 —
Neurocrine Clinical Site North Canton Ohio 44730 —
Neurocrine Clinical Site Houston Texas 77008 —
Neurocrine Clinical Site Richardson Texas 75080 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06267846, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 17, 2026 · Synced Oct 11, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06267846 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →