ClinicalTrials.gg
CompletedNCT01941043Updated Dec 21, 2017

A Randomized, Double-Blind, Placebo-Controlled, Sequential Parallel Study of CERC-301 in the Adjunctive Treatment of Subjects With Severe Depression and Recent Active Suicidal Ideation Despite Antidepressant Treatment

A Phase 2 interventional study of CERC-301 and Placebo in Major Depressive Disorder, sponsored by Avalo Therapeutics, Inc.. Completed at 24 sites in United States. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2017-12-21.

Sponsored by Avalo Therapeutics, Inc. · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
1,357
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
All
01

Study summary

The current study will evaluate the antidepressant effect of CERC-301 during 28 days of treatment in subjects with MDD who are currently experiencing a severe depressive episode despite stable ongoing treatment with selective serotonin- or serotonin-norepinephrine reuptake inhibitors (SSRI or SNRI). The study population will be enriched for subjects that would benefit most from rapid onset, those with recent active suicidal ideation, but not a risk to themselves or others and are deemed appropriate for an out-patient study with careful safety surveillance. This will allow the study to focus on the antidepressant effects of CERC-301 but also explore effects on suicidal ideation. To explore rapid onset, the primary endpoint will be at 7 days, but effects over the 28 days of treatment will be examined as a secondary endpoint.

02

Conditions studied

  • Major Depressive Disorder
03

In context

Depressive Disorder, Major

3,041 studies on the registry are indexed under Depressive Disorder, Major; 588 are open to participants now.

This study's enrollment of 1,357 is above the median of 79 across 2,530 interventional studies indexed under Depressive Disorder, Major.

Browse Depressive Disorder, Major studies →

Lead sponsor

Avalo Therapeutics, Inc. is the lead sponsor of 10 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Male or female 18 to 70 years of age inclusive.
  2. Females must be either:

    1. (amenorrhea for at least 12 consecutive months), surgically sterile -or-
    2. Women of (WOCBP) meeting the criteria below:

    i. Uses an acceptable double-barrier method of as determined by the Investigator -and- ii. Is not lactating, has a negative serum beta human chorionic gonadotropin pregnancy test at screening and a negative urine pregnancy test prior to randomization on Day 0.

  3. Male subjects must agree to use a condom if partner is of childbearing potential.
  4. Diagnosis of MDD recurrent without psychotic features according to , Fourth Edition, Text Revision (DSM-IV-TR) criteria with diagnosis confirmed using the Structured Clinical Interview for DSM-IV Axis I Disorders Clinical Trials Version (SCID-CT).
  5. Currently adhering to antidepressant drug regimen that consists of stable SSRI or SNRI therapy
  6. Inadequate antidepressant response to current antidepressant therapy despite adequate dose and duration
  7. HDRS-17 score ≥ 21 on the HDRS-17 performed by the site at screening
  8. Recent active suicidal ideation defined as a score of 2 on the intensity of ideation section on the Columbia-Suicide Severity Rating Scale (C-SSRS) during the four weeks prior to screening using the "Baseline/Screening" version of the C-SSRS.
  9. In otherwise good general health without any unstable medical conditions (as determined by medical history, physical examination, 12-lead , clinical laboratory testing, etc.).

Exclusion criteria

Exclusion Criteria:

  1. History of substance abuse or dependence within the 3 months prior to screening.
  2. Positive urine drug test at screening and prior to randomization on Day 0 unless due to a permitted medication that is documented in the subject's medication history.
  3. Positive ethanol breath test at screening and/or prior to randomization on Day 0.
  4. Elevated semi-recumbent blood pressure at screening and prior to randomization on Day 0, defined as systolic blood pressure > 140 mm Hg and diastolic blood pressure
  5. Active, comorbid disease that might limit the ability of the subject to participate in the study as determined by the Investigator (i.e. poorly controlled diabetes mellitus, unstable angina, coronary artery disease, congestive heart failure, etc.).
  6. Subjects with clinical laboratory test abnormality deemed by the Investigator at screening.
  7. Axis I diagnosis of obsessive compulsive disorder, posttraumatic stress disorder, bipolar I or II mood disorders, eating disorders (e.g., anorexia nervosa, bulimia nervosa), psychotic disorders (e.g., schizoaffective disorder, schizophrenia), significant cognitive disorders (e.g., delirium, dementia, amnesia), or dissociative disorders.
  8. Subjects with Axis II diagnosis of borderline, antisocial, paranoid, schizoid, schizotypal, or histrionic personality disorder.
  9. Subjects with a neurologic disorder that could cause or contribute to depression (e.g., Alzheimer's disease, Parkinson's disease).
  10. Female subjects currently experiencing postpartum depression.
  11. Subjects who, in the opinion of the Investigator, are not appropriate for a 35-day placebo-controlled study due to risk of significant threat to self or others during screening or study conduct.
  12. Use of other NMDA-receptor modulators (e.g., dextromethorphan, ketamine, amantadine, memantine) within 30 days of screening and throughout the study.
  13. The following concomitant medication use is excluded within six weeks prior to screening:

    • Bupropion or tricyclic antidepressants
    • Intermittent, symptomatic use of benzodiazepines (e.g. symptomatic treatment of anxiety or panic attacks)
    • Antipsychotics
    • Lithium
    • Any medications known to directly interact with central or peripheral serotonergic receptors, other than the permitted antidepressants.
    • Any medications known to directly interact with central noradrenergic receptors, other than the permitted antidepressants.
  14. Electroconvulsive therapy, transcranial magnetic stimulation, or vagal nerve stimulation during the current depressive episode.
  15. Participation in an drug or device study within the 6 months prior to screening.
  16. Subjects with suicidal behavior within 6 months prior to screening as measured by the C-SSRS "Baseline/Screening" version.
  17. Subjects with a C-SSRS score > 2 on the intensity of ideation section at randomization (Visit 2a), using the "Since Last Visit" version of the C-SSRS.
Terms in these criteria, in plain language(7)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

ECG (electrocardiogram)

A recording of the heart’s electrical activity, taken with stickers on the chest, arms and legs. It takes a few minutes and does not hurt.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
1,357 participants (actual)

Study arms

  • Experimental
    CERC-301, Treatment Sequence 1

    Treatment Sequence 1 - 7 days on placebo and 28 days on study drug (either 12mg or 8mg)

    Drug: CERC-301 · Other: Placebo

  • Experimental
    CERC-301, Treatment Sequence 2

    Treatment Sequence 2 - Placebo for 7 days and study drug for 28 days (8 mgs)

    Drug: CERC-301 · Other: Placebo

  • Placebo comparator
    Placebo, Treatment Sequence 3

    Treatment Sequence 3 - Placebo for 35 Day treatment period

    Other: Placebo

Interventions

06

What researchers measure

Primary outcomes

  1. HDRS-17 after 7 days of dosing with study drug

    The overall between-treatment difference will be computed as the weighted average of the differences (drug vs. placebo)

    Time frame: Screening & Days 0, 4, 7, 11, 14, 21,28, & 35

Secondary outcomes

  1. HDRS-17 Averaged between 7 and 28 days of treatment with study drug

    This will be analyzed using the mixed effects model for repeated measures. The between-group (drug vs. placebo) differences will be estimated by the least squares mean for the contrast in the main effect.

    Time frame: Screening, Days 0, 4, 7, 11, 14, 21, 28, & 35

  2. HDRS-17 after 28 days of dosing with study drug

    This will be analyzed using the mixed effects model for repeated measures . The between-group difference will be estimates by the least squares mean difference at Day 28 as a simple contrast from the model.

    Time frame: Screening, Days 0, 4, 7, 11, 14, 21, 28, 35

07

Study locations

24 sites
  • University of Alabama at Birmingham
    Birmingham, Alabama 35294, United States
  • Arizona TMS Therapy Center
    Phoenix, Arizona 85032, United States
  • ProScience Research Group
    Culver City, California 90230, United States
  • Collaborative NeuroScience Network, Inc.
    Garden Grove, California 92845, United States
  • Behavioral Research Specialists
    Glendale, California 91206, United States
  • Synergy Clinical Research Center
    National City, California 91950, United States
  • Pacific Clinical Trials, LLC
    Oakland, California 94612, United States
  • Southern CA Psychiatrists
    Oceanside, California 92056, United States
  • Artemis Institute for Clinical Research
    San Diego, California 92123, United States
  • Clinical Neuroscience Solutions
    Jacksonville, Florida 32256, United States
  • Scientific Clinical Research, Inc.
    North Miami, Florida 33161, United States
  • Clinical Neuroscience Solutions
    Orlando, Florida 32806, United States
  • Atlanta Center for Medical Research
    Atlanta, Georgia 30308, United States
  • Northwest Behavioral Research Center
    Marietta, Georgia 30060, United States
  • Chicago Psychiatry Associates
    Chicago, Illinois 60602, United States
  • Sheppard Pratt Health System
    Baltimore, Maryland 21285, United States
  • PCRC
    O'Fallon, Missouri 63368, United States
  • Bioscience Research
    Mount Kisco, New York 10549, United States
  • The Medical Research Network
    New York, New York 10128, United States
  • Finger Lakes Clinical Research
    Rochester, New York 14618, United States
  • Neuro-Behavioral Clinical Research, Inc.
    Canton, Ohio 44718, United States
  • Suburban Research Associates
    Media, Pennsylvania 19063, United States
  • FutureSearch Trials of Dallas
    Dallas, Texas 75231, United States
  • Northwest Clinical Research Center
    Bellevue, Washington 98007, United States
08

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Nov 2013, a primary completion of Sep 2014 and a completion of Oct 2014. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 5, 2013
First posted
Sep 13, 2013
Start
Nov 2013
Primary completionActual
Sep 2014
CompletionActual
Oct 2014
Results delay requested
Sep 18, 2017
Last update
Dec 21, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 21, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01941043
Lead sponsor
Avalo Therapeutics, Inc.
Responsible party
Sponsor
First posted
Sep 13, 2013
Start date
Nov 2013
Primary completion
Sep 2014
Completion
Oct 2014
Last update
Dec 21, 2017

Study contacts

James Vornov, MD, PhD
study director · Avalo Therapeutics, Inc.

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

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Studies of the drug tested here: Rislenemdaz

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