Double-Blind Trial of Ketamine Therapy Plus or Minus Naltrexone in Treatment Resistant Depression (TRD)

The primary goal is to determine if the antidepressant effects of Ketamine are mediated by an
opiate mechanism.

Primary Objective:

To determine if the opioid properties of Ketamine are responsible for it's antidepressant
effects by potentially blocking the antidepressant effects with a opioid antagonist
naltrexone.

We will measure this objective by looking at the response on a scale called the 6- item
Hamilton Rating Scale for Depression (HAM-D-6). Response is defined as a statistically
significant greater decrease on the overall score on this scale, post infusion.

Secondary Objective:

This includes comparing a scale called Clinician Administered Dissociative States Scale
(CADSS) on both of our patient groups, one group receiving Ketamine plus Naltrexone compared
to the other group receiving Ketamine plus placebeo, to determine if naltrexone has any
effect on CADSS as well as to determine if CADSS is associated with antidepressant response

Another secondary objective is to assess ketamine craving using the Visual Analog Craving
Scale for Ketamine (VASK), after infusion and determine if there is a change in level of
craving for the group that receives naltrexone.

Number of Subjects:

i) 30

ii) The subjects will be drawn from an outpatient sample of patients with MDD, diagnosed with
the use of the Structured Clinical Interview for DSM-IV Axis I Disorders(SCID-I/P), currently
on a stable, adequate dose of antidepressant therapy, as defined by the MGH ATRQ, for at
least 4 weeks or a history of intolerance to at least 2 antidepressant treatments.

Inclusion Criteria:

A subject will be eligible for inclusion only if all of the following criteria are met:

1. Male or female, 18 to 70 years of age, inclusive, at screening.

2. Able to read, understand, and provide written, dated informed consent prior to
screening. Participants will be deemed likely to comply with study protocol and
communicate with study personnel about adverse events and other clinically important
information.

3. 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, according to the criteria defined in the Diagnosis and Statistical
Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR™). The diagnosis
of MDD will be made by a site psychiatrist and supported by the Structured Clinical
Interview for DSM-IV-TR™ (SCID-I/P) or the M.I.N.I International Neuropsychiatric
Interview a short, structured psychiatric interview.

4. Has a history of TRD during the current MDE, as assessed by the investigator. TRD is
defined as failure to achieve a satisfactory response (e.g., less than 50% improvement
of depression symptoms), as perceived by the participant, to at least two "treatment
courses" of a therapeutic dose of an antidepressant therapy of at least 8 weeks
duration. The adequacy of dose and duration of the antidepressant therapy will be
determined as per the Massachusetts General Hospital Antidepressant Treatment Response
Questionnaire (MGH ATRQ) criteria. Participants must currently be on a stable (for at
least 4 weeks) and adequate (according to the MGH ATRQ) dose of ongoing Selective
serotonin reuptake inhibitor (SSRI) or Serotonin-norepinephrine reuptake inhibitor
(SNRI) antidepressant therapy, of which total duration must be at least 8 weeks.
Participants may also have a history of intolerance to at least 2 antidepressant
medications. These patients with the intolerance history will not be required to be
currently taking an antidepressant medication.

5. Meet the threshold on the total Hamilton Depression 17-item Scale (HAMD17) score of
>/=20 at both screening and baseline visits (Day -5/-14 and Day 0).

6. In good general health, as ascertained by medical history, physical examination (PE)
(including measurement of supine and standing vital signs), clinical laboratory
evaluations, and 12-lead electrocardiogram (ECG).

7. If female, a status of non-childbearing potential or use of an acceptable form of
birth control per the following specific criteria:

1. Non-childbearing potential (e.g., physiologically incapable of becoming pregnant,
i.e., permanently sterilized (status post hysterectomy, bilateral tubal
ligation), or is post-menopausal with her last menses at least one year prior to
screening); or

2. Childbearing potential, and meets the following criteria:

i. Childbearing potential, including women using any form of hormonal birth control,
on hormone replacement therapy started prior to 12 months of amenorrhea, using an
intrauterine device (IUD), having a monogamous relationship with a partner who has had
a vasectomy, or is sexually abstinent.

ii.Negative urinary pregnancy test at screening, confirmed by a negative urinary
pregnancy test at randomization prior to receiving study treatment.

iii.Willing and able to continuously use one of the following methods of birth control
during the course of the study, defined as those which result in a low failure rate
(i.e., less than 1% per year) when used consistently and correctly: implants,
injectable or patch hormonal contraception, oral contraceptives, IUD, double-barrier
contraception, sexual abstinence. The form of birth control will be documented at
screening and baseline.

8. Body mass index between 18-35kg/m2.

9. Concurrent psychotherapy will be allowed if the type (e.g., supportive, cognitive
behavioral, insight-oriented, et al) and frequency (e.g., weekly or monthly) of the
therapy has been stable for at least three months prior to screening and if the type
and frequency of the therapy is expected to remain stable during the course of the
subject's participation in the study.

10. Concurrent hypnotic therapy (e.g., with zolpidem, zaleplon, melatonin, or trazodone)
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:

A potential participant will NOT be eligible for participation in this study if any of the
following criteria are met:

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

2. Female that is pregnant or breastfeeding.

3. Female with a positive pregnancy test at screening or baseline.

4. Total HAMD score of <20 at the screen or baseline visits.

6. Current diagnosis of a Substance Use Disorder (Abuse or Dependence, as defined by
DSM-IV-TR™), with the exception of nicotine dependence, at screening or within six months
prior to screening.

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

8. History of schizophrenia or schizoaffective disorders, or any history of psychotic
symptoms in the current or previous depressive episodes.

9. History of anorexia nervosa, bulimia nervosa, or eating disorder not otherwise
specified, within five years of screening.

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

11. Considered at significant risk for suicide during the course of the study according to
any of the following criteria:

12. In the judgment of the investigator, the subject is at significant risk for suicidal
behavior during the course of his/her participation in the study.

13. Has dementia, delirium, amnestic, or any other cognitive disorder.

14. Has a clinically significant abnormality on the screening physical examination that
might affect safety, study participation, or confound interpretation of study results.

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

16. Known history or current episode of:

a. QTcF (a measure of the time between the start of the Q wave and the end of the T wave in
the heart's electrical cycle-Fridericia-corrected) ≥450 msec at screening (Visit 1) or
randomization b. Syncopal event within the past year. c. Congestive heart failure (CHF) New
York Heart Association Criteria >Stage 2 d. Angina pectoris e. Heart rate <50 or >105 beats
per minute at screening or randomization

17. Chronic lung disease.

18. Lifetime history of surgical procedures involving the brain or meninges, encephalitis,
meningitis, degenerative central nervous system disorder (e.g., Alzheimer's or Parkinson's
Disease), epilepsy, mental retardation, or any other
disease/procedure/accident/intervention associated with significant injury to or
malfunction of the central nervous system (CNS), or a history of significant head trauma
within the past two years.

19. Presents with any of the following lab abnormalities w/in the past 6 months:

1. Thyroid stimulating hormone (TSH) outside of the normal limits and clinically
significant as determined by the investigator. Free thyroxine (T4) levels may be
measured if TSH level is high. Subject will be excluded if T4 level is clinically
significant.

2. Any other clinically significant abnormal laboratory result at the time of the
screening exam.

20. History of hypothyroidism and has been on a stable dosage of thyroid replacement
medication for less than six months prior to screening.(Subjects on a stable dosage of
thyroid replacement medication for at least six months or more prior to screening are
eligible for enrollment.)

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

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

23. History of positive screening urine test for drugs of abuse at screening: cocaine,
amphetamines, barbiturates, opiates.

24. Chronic use of opiates.