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Clinical Trials/NCT01941043
NCT01941043
Completed
Phase 2

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

Avalo Therapeutics, Inc.23 sites in 1 country1,357 target enrollmentNovember 2013

Overview

Phase
Phase 2
Intervention
CERC-301
Conditions
Major Depressive Disorder
Sponsor
Avalo Therapeutics, Inc.
Enrollment
1357
Locations
23
Primary Endpoint
HDRS-17 after 7 days of dosing with study drug
Status
Completed
Last Updated
8 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
October 2014
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male or female 18 to 70 years of age inclusive.
  • Females must be either:
  • Post-menopausal (amenorrhea for at least 12 consecutive months), surgically sterile -or-
  • Women of childbearing potential (WOCBP) meeting the criteria below:
  • i. Uses an acceptable double-barrier method of contraception 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
  • Male subjects must agree to use a condom if partner is of childbearing potential.
  • Diagnosis of MDD recurrent without psychotic features according to Diagnostic and Statistical Manual of Mental Disorders, 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).
  • Currently adhering to antidepressant drug regimen that consists of stable SSRI or SNRI therapy
  • Inadequate antidepressant response to current antidepressant therapy despite adequate dose and duration
  • HDRS-17 score ≥ 21 on the HDRS-17 performed by the site at screening

Exclusion Criteria

  • History of substance abuse or dependence within the 3 months prior to screening.
  • 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.
  • Positive ethanol breath test at screening and/or prior to randomization on Day
  • 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
  • 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.).
  • Subjects with clinical laboratory test abnormality deemed clinically significant by the Investigator at screening.
  • 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.
  • Subjects with Axis II diagnosis of borderline, antisocial, paranoid, schizoid, schizotypal, or histrionic personality disorder.
  • Subjects with a neurologic disorder that could cause or contribute to depression (e.g., Alzheimer's disease, Parkinson's disease).
  • Female subjects currently experiencing postpartum depression.

Arms & Interventions

CERC-301, Treatment Sequence 1

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

Intervention: CERC-301

CERC-301, Treatment Sequence 1

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

Intervention: Placebo

CERC-301, Treatment Sequence 2

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

Intervention: CERC-301

CERC-301, Treatment Sequence 2

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

Intervention: Placebo

Placebo, Treatment Sequence 3

Treatment Sequence 3 - Placebo for 35 Day treatment period

Intervention: Placebo

Outcomes

Primary Outcomes

HDRS-17 after 7 days of dosing with study drug

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

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

Secondary Outcomes

  • HDRS-17 after 28 days of dosing with study drug(Screening, Days 0, 4, 7, 11, 14, 21, 28, 35)
  • HDRS-17 Averaged between 7 and 28 days of treatment with study drug(Screening, Days 0, 4, 7, 11, 14, 21, 28, & 35)

Study Sites (23)

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