Proof-of-Concept Trial of CERC-501 Augmentation of Antidepressant Therapy in Treatment-Resistant Depression

This study will involve 10 visits to the clinical site over approximately 1.5 months. There
will be a screening visit (7-28 days may pass between the screening visit and the first
treatment visit), a baseline/treatment visit (first day of study drug treatment), followed
by 5 consecutive days of treatment visits. Follow-up visits will occur 6, 13, and 20 days
after first receiving study drug.

Inclusion Criteria:

- Male or female, 18-65 years old.

- Able to read, understand, and provide written, dated informed consent prior to
screening.

- Diagnosed with Major Depressive Disorder (MDD), single or recurrent, and currently
experiencing a Major Depressive Episode (MDE) of at least eight weeks in duration,
prior to screening.

- Has a history of treatment resistance during the current MDE.

- Meet the threshold on the total MADRS score of greater than or equal to 20 at both
screening and baseline visits, as confirmed by the remote centralized MGH CTNI rater
between the screen visit and the baseline visit.

- In good general health

- For female participants, status of non-childbearing potential or use of an acceptable
form of birth control

- Body mass index between 18-40 kg/m2

- Concurrent psychotherapy will be allowed if the type and frequency of the therapy has
been stable for at least three months prior to screening and is expected to remain
stable during participation in the study

- Concurrent benzodiazepine and hypnotic therapy will be allowed if the therapy has
been stable for at least 4 weeks prior to screening and if it is expected to remain
stable during the course of the subject's participation in the study.

Exclusion Criteria:

- Female of childbearing potential who is not willing to use one of the specified forms
of birth control during the study

- Female that is pregnant or breastfeeding

- Female with a positive pregnancy test at screening or baseline

- History during the current MDE of failure to achieve a satisfactory response to >3
treatment courses of a therapeutic dose of an antidepressant therapy of at least 8
weeks duration during the current episode

- Total MADRS score of <20 at the screen or baseline visits, or as assessed by the
remote, independent MGH CTNI rater and reported to the site

- Current diagnosis of a Substance Use Disorder (Abuse or Dependence) with the
exception of nicotine dependence, at screening or within six months prior to
screening

- Current diagnosis of Axis I disorders other than Dysthymic Disorder, Generalized
Anxiety Disorder, Social Anxiety Disorder, Panic Disorder or Specific Phobia (unless
one of these is comorbid and clinically unstable, and/or the focus of the
participant's treatment for the past 6 months or more)

- History of bipolar disorder, schizophrenia or schizoaffective disorders, or any
history of psychotic symptoms in the current or previous depressive episodes

- History of eating disorders within five years of screening

- Any Axis I or Axis II Disorder, which at screening is clinically predominant to their
MDD or has been predominant at any time within 6 months prior to screening

- Subject is considered at significant risk for suicidal behavior during the course of
their participation in the study

- Subject has had electroconvulsive therapy in the current episode of depression

- Has received vagus nerve stimulation (VNS) at any time prior to screening

- Dementia, delirium, amnestic, or any other cognitive disorder

- Has a clinically significant abnormality on the screening physical examination

- Participation in any clinical trial with an investigational drug or device within the
past month or concurrent to study participation

- Known history or current episode of: Uncontrolled hypertension, Recent myocardial
infarction (within one year) or a history of more than one myocardial infarction,
Syncopal event within the past year, Congestive heart failure, Angina pectoris,
Systolic BP <85 or >160 mmHg or diastolic BP >95 mmHg or heart rate <50 or >105 beats
per minute at screening or randomization, or QTcF greater than or equal to 450 msec
at screening or randomization.

- Chronic lung disease

- Lifetime history of surgical procedures involving the brain or meninges,
encephalitis, meningitis, degenerative central nervous system disorder, epilepsy,
mental retardation, or any other disease/procedure/accident/intervention associated
with significant injury to or malfunction of the central nervous system, or a history
of significant head trauma within the past 2 years

- Presents with a history of Thyroid stimulating hormone outside of the normal limits
and clinically significant as determined by the investigator

- Patients with diabetes mellitus fulfilling any of the following criteria:

1. Unstable diabetes mellitus defined as glycosylated hemoglobin (HbA1c) >8.5% at
screening

2. Admitted to hospital for treatment of diabetes mellitus or diabetes mellitus
related illness in the past 12 weeks

3. Not under physician care for diabetes mellitus

4. Has not been on the same dose of oral hypoglycaemic drug(s) and/or diet for the
4 weeks prior to screening. For thiazolidinediones (glitazones) this period
should not be less than 8 weeks.

5. Any other clinically significant abnormal laboratory result (as determined after
evaluation by study investigator and MGH CTNI medical monitor) at the time of
the screening exam.

- History of hypothyroidism and has been on a stable dosage of thyroid replacement
medication, or was surgically treated less than six months prior to screening

- History of hyperthyroidism which was treated (medically or surgically) less than six
months prior to screening

- Any current or past history of any physical condition which in the investigator's
opinion might put the subject at risk or interfere with the interpretation of study
results

- History of positive screening urine test for drugs of abuse

- Patients with exclusionary laboratory values, or requiring treatment with
exclusionary concomitant medications, including tricyclic antidepressants and
monoamine oxidase inhibitors, or on two or more concomitant antidepressant therapies

- Patients currently taking a proton pump inhibitor (PPI)/histamine 2 (H2) blocker or
with a history of chronic NSAID use

- Patients with a positive test for Helicobacter pylori (urea breath test)

- Patients with any of the following GI-related findings:

1. Clinically evident GI complaints or GI disease at Screening or Visit 1

2. Past history of gastric disease (including but not limited to peptic ulcer
disease, gastritis (including atrophic gastritis), upper GI bleeding, any other
GI precancerous conditions), and of any other clinically relevant GI disease.