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Recruiting Phase 2

ACP-211 Monotherapy for Major Depressive Disorder With Inadequate Antidepressant Response

NCT07284667 · tracked via the Priya Life Science USA tracker
Phase
Phase 2
Started
2025-11-14
Last updated
2026-10-05

Condition(s) studied

Major Depressive Disorder (MDD)Depressive Disorder, Treatment-Resistant

Investigational drug(s) / intervention(s)

ACP-211Placebo

ACP-211: ACP-211 monotherapy

Placebo: Placebo control

Study summary

The goal of this clinical trial is to learn if ACP-211 can help treat adults with major depressive disorder (MDD) who have not improved with antidepressant therapy (ADT), including those with treatment resistant depression (TRD).

The main questions the study aims to answer are:

* Does ACP-211 work better than a placebo (a look-alike capsule with no medicine) to reduce symptoms of depression?
* What adverse events do participants have when taking ACP-211?

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Adults ≥18 and ≤65 years of age * Provides written informed consent * Clinical diagnosis of MDD * History of inadequate response to at least two antidepressants, with at least one inadequate response documented during the current episode * Currently treated with an approved antidepressant at a stable dose prior to Screening * MADRS total score ≥28, CGI-S score ≥4 , and QIDS-SR16 score ≥16 at Screening and Baseline * Females of childbearing potential must have a negative pregnancy test and agree to use acceptable contraception; males must agree to use barrier protection and refrain from sperm donation Exclusion Criteria: * Current diagnosis of certain personality disorders or persistent depressive disorder * Recent substance use disorders, excluding caffeine or nicotine * Active suicidal risk or recent suicidal attempt * History of schizophrenia, psychotic disorders, bipolar disorder, or MDD with psychotic features * Current treatment requirement for PTSD, acute stress disorder, panic disorder, or OCD * History of neuroleptic malignant syndrome, serotonin syndrome, or epilepsy (except single febrile seizure in infancy) * Allergy or sensitivity to ketamine or esketamine * Significant cardiovascular disease * Positive history of hepatitis B, hepatitis C, or HIV infection * Unstable diabetes or uncontrolled medical conditions * Positive urine drug test for an illicit drug or cannabis * Received neuromodulation therapies (ECT, TMS, VNS, DBS) in the current depressive episode * Recent initiation or change in psychotherapy Additional inclusion/exclusion criteria apply. Participants will be evaluated at Screening to ensure that all criteria for study participation are met.

Primary outcome measure(s)

  • Change From Baseline in Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score at Day 28 — Baseline and Day 28
    The MADRS is a clinician-rated scale that assesses the severity of depressive symptoms. It consists of 10 items, each scored from 0 (no symptoms) to 6 (severe symptoms), resulting in a total score range of 0 to 60. Higher scores indicate greater depression severity.

Trial sites (28)

FacilityCityRegionStatus
University of Alabama at Birmingham Birmingham Alabama Withdrawn
Inland Psychiatric Medical Group Chino California Recruiting
Behavioral Research Specialists, LLC Glendale California Recruiting
Kadima Neuropsychiatry Institute La Jolla California Recruiting
PNS Clinical Research LLC dba ATP Clinical Research Orange California Recruiting
Focus Clinical Research, LLC d/b/a Alliance Clinical West Hills West Hills California Recruiting
Mountain View Clinical Research Denver Colorado Recruiting
New Access Research and Medical Services, Inc. Fort Myers Florida Recruiting
The Medici Medical Research Hollywood Florida Recruiting
Sandhill Research, LLC/DBA Accel Research Sites Largo Florida Withdrawn
Clinical Neuroscience Solutions, Inc. Orlando Florida Recruiting
IPTB Clinical Research Tampa Florida Recruiting
Neuroscience Research Institute, Inc. West Palm Beach Florida Recruiting
Adams Clinical, Inc. Watertown Massachusetts Recruiting
Vitalix Clinical, Inc. Worcester Massachusetts Recruiting
Precise Research Centers Flowood Mississippi Recruiting
St. Charles Psychiatric Associates, Inc. dba Midwest Research Group Saint Charles Missouri Recruiting
Alivation Research, LLC Lincoln Nebraska Recruiting
Redbird Research LLC Las Vegas Nevada Recruiting
CenExel Hassman Research Institute, LLC Marlton New Jersey Withdrawn
Integrative Clinical Trials LLC Brooklyn New York Recruiting
Magnolia Clinical Research, LLC Cary North Carolina Recruiting
Neuro-Behavioral Clinical Research North Canton Ohio Recruiting
Baylor College of Medicine Houston Texas Recruiting
Dynamed Clinical Research LP d/b/a DM Clinical Research Houston Texas Withdrawn
Olympus Clinical Research, LLC Katy Texas Recruiting
Family Psychiatry of The Woodlands The Woodlands Texas Recruiting
Aura Wellness Salt Lake City Utah Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07284667 on ClinicalTrials.gov ↗ ← All trials in the USA