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NCT06911112 · ClinicalTrials.gov registry record · Phase 3

NBI-1065845-MDD3025: Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

A Phase 3 study of Major Depressive Disorder, sponsored by Neurocrine Biosciences.

Recruiting
Registry status
Phase 3
Development phase
200
Enrollment target
10
Study locations

NCT06911112 is a Phase 3 study of Major Depressive Disorder that is actively recruiting participants, run by Neurocrine Biosciences. The registered enrollment target is 200 participants, below the 376-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (47% lower). The trial reports 10 study locations across 8 states.

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The verdict

NCT06911112, a Phase 3 study of Major Depressive Disorder, is actively recruiting participants, sponsored by Neurocrine Biosciences.

RECRUITING
Registry status
Phase 3
Development phase
200 participants
Enrollment target
10
Study locations

Study Summary

The study will evaluate the efficacy of NBI-1065845 compared with placebo as an adjunctive treatment in participants with MDD on improving symptoms of depression.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG NBI-1065845

Study Locations (10)

California

  • Neurocrine Clinical Site - Glendale
  • Neurocrine Clinical Site - Irvine

Florida

  • Neurocrine Clinical Site - Miami
  • Neurocrine Clinical Site - Tampa

Alabama

  • Neurocrine Clinical Site - Huntsville

Georgia

  • Neurocrine Clinical Site - Atlanta

Massachusetts

  • Neurocrine Clinical Site - Boston

Missouri

  • Neurocrine Clinical Site - Saint Charles

New York

  • Neurocrine Clinical Site - The Bronx

Ohio

  • Neurocrine Clinical Site - Mason

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2025-03-31
Est. Completion 2027-07
Phase Phase 3

Sponsor

Neurocrine Biosciences

65 total trials

What the Registry Record Tells You About NCT06911112

The ClinicalTrials.gov registry entry for NCT06911112 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 376-participant average among 282 other Major Depressive Disorder trials with a reported enrollment target (47% lower). The listed sponsor is Neurocrine Biosciences, which has 65 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Major Depressive Disorder appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT06911112 reports 10 study locations spanning 8 distinct geographic areas - top geographies include California, Florida, Alabama.

Frequently Asked Questions

What is clinical trial NCT06911112 about?

NCT06911112 is a clinical study titled "NBI-1065845-MDD3025: Study to Assess the Efficacy and Safety of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)". The study will evaluate the efficacy of NBI-1065845 compared with placebo as an adjunctive treatment in participants with MDD on improving symptoms of depression.

What is the current status of trial NCT06911112?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 200 participants. The study started on 2025-03-31. Estimated completion is 2027-07.

What conditions does trial NCT06911112 study?

This clinical trial studies the following conditions: Major Depressive Disorder.

What interventions are being tested in trial NCT06911112?

The interventions under investigation include: Placebo (DRUG), NBI-1065845 (DRUG).

Who is sponsoring clinical trial NCT06911112?

This trial is sponsored by Neurocrine Biosciences, which has 65 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06911112 being conducted?

This trial has 10 study locations across Alabama, California, Florida, Georgia, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.