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Completed Phase 2 Interventional

A Study of Intermittent Doses of CERC-301 in MDD

ClinicalTrials.gov ID: NCT02459236

Public ClinicalTrials.gov record NCT02459236. 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 Sep 10, 2026, 6:42 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 Randomized, Double-Blind, Placebo-Controlled Study of Intermittent Doses of CERC-301 in the Treatment of Subjects With Severe Depression Despite Antidepressant Treatment

Brief summary

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

There is a significant unmet medical need for rapidly acting treatment of subjects with severe major depressive disorder (MDD) who have not adequately responded to antidepressant therapy. Alternative therapies require weeks to achieve full efficacy, may have significant side effects, and still fail in a high percentage of subjects. Rapid reduction of severe depression by pharmacological therapy is important to reduce the need for hospitalization and risk of self-harm and mortality. CERC-301, a highly selective, orally bioavailable, N-methyl-D-aspartate (NMDA) receptor subunit 2B (NR2B), also referred to as Glutamate NMDA receptor subunit epsilon-2 (GluN2B) antagonist, would be a therapeutic breakthrough if it provides rapid onset of antidepressant effects and an effect size similar to that seen with experimental intravenous NMDA modulators.

Study identification

NCT ID
NCT02459236
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Avalo Therapeutics, Inc.
Industry
Enrollment
115 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
May 31, 2015
Primary completion
Aug 31, 2016
Completion
Nov 30, 2016
Last update posted
Sep 27, 2017

2015 – 2016

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Pharmacology Research Institute (PRI) Newport Beach California 92660
Institute for Advanced Medical Research Alpharetta Georgia 30005
Chicago Research Center, Inc. Chicago Illinois 60634
Alexian Brothers Center for Psychiatric Research Hoffman Estates Illinois 60169
Psychiatric Care and Research Center O'Fallon Missouri 63368
Bioscience Research LLC Mount Kisco New York 10549
The Medical Research Network, LLC New York New York 10128
Fingerlakes Clinical Research Rochester New York 14618
Richmond Behavioral Associates Staten Island New York 10312
Summit Research Network (Oregon) Inc. Portland Oregon 97201
Lehigh Center for Clinical Research Allentown Pennsylvania 18104
Research Strategies of Memphis, LLC Memphis Tennessee 38119
Northwest Clinical Research Center Bellevue Washington 98007

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 NCT02459236, 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 Sep 27, 2017 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02459236 live on ClinicalTrials.gov.

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