Efficacy of H7-Coil DTMS Compared to H1-Coil DTMS in Subjects With Major Depression Disorder (MDD)

This is a prospective, 6 week, double blind, randomized, controlled, multi-center trial. The
study will explore the safety and efficacy of deep brain rTMS (Transcranial Magnetic
Stimulation) H7-Coil treatment and demonstrate that it is as good as the FDA cleared, H1-Coil
treatment as add-on for a treatment with antidepressant drugs (a bi-therapeutic treatment )
in subjects with major depressive disorder that have been previously unsuccessfully treated
with antidepressant medication.

Approximately 106 subjects will be enrolled in the study. The study population consists of
subjects with MDD who have failed adequate medication treatment and who are in a current
depressive episode.

The patients will be of all racial, ethnic and gender categories, ranging from 22 to 68 years
of age, and have HDRS-21≥20. Outpatients will be recruited from both academic and private
research centers.

The study duration is 8 weeks, with a 2 week period of screening and baseline, followed by 4
weeks of 5 daily treatments and 2 weeks of biweekly treatments. Mood and mental state will be
carefully monitored through standard psychological scales and assessments during the
screening and baseline and throughout treatment.

Inclusion Criteria:

- Outpatients

- Men and women 22-68 years of age

- Primary DSM-IV diagnosis of Major Depression, single or recurrent episode.

- Current depressive episode is less than 5 years duration

- The patient did not respond to at least one but not more than four antidepressant
treatments in the current episode or Patients who have not completed antidepressant
trials due to intolerance to therapy of 2 or more anti-depressant medications in the
current episode

- Satisfactory safety screening questionnaire for transcranial magnetic stimulation

- Patients not suffering from hypo or hyper-thyroidism based on pre-study TSH level or
medically stabilized

- Capable and willing to provide informed consent and able to adhere to the treatment
schedule

- Patient is stable on medication for 2 month and is not expected to change medication
during all study period

Exclusion Criteria:

- Individuals diagnosed by the Investigator with the following conditions (current
unless otherwise stated):

- Depression secondary to a general medical condition, or substance-induced

- History of substance abuse or dependence within the past 6 month (except nicotine
and caffeine)

- Any psychotic disorder (lifetime), including schizoaffective disorder, or major
depression with psychotic features, Bipolar disorder, Eating disorder, Obsessive
compulsive disorder

- Post-traumatic stress disorder (current or within the past year)

- Current generalized anxiety disorder, panic disorder or social anxiety disorder

- Presence of a personality disorder (such as antisocial, schizotypal, histrionic,
borderline, narcissistic)

- Individuals with a significant neurological disorder or insult including, but not
limited to:

- Any condition likely to be associated with increased intracranial pressure

- Space occupying brain lesion

- Any history of seizure EXCEPT those therapeutically induced by ECT

- History of cerebrovascular accident

- Transient ischemic attack within two years

- Cerebral aneurysm

- Dementia

- Mini Mental State Exam score of less than or equal to 24

- Parkinson's disease

- Huntington's chorea

- Multiple sclerosis

- Increased risk of seizure for any reason

- Individuals with hearing loss

- ECT treatment within 3 months prior to the screening visit

- History of treatment with Vagus Nerve Stimulation (VNS)

- History of treatment with Deep Brain Stimulation (DBS)

- Use of any investigational drug within 4 weeks of the randomization visit

- Use of any prohibited study medication(s)

- Present suicidal risk as assessed by the investigator or significant suicide risk

- Any self-inflicted harm in the past 3 months not in the context of suicidal ideation

- Cardiac pacemakers, implanted medication pumps, intracardiac lines, or acute, unstable
cardiac disease

- Intracranial implant (e.g., aneurysm clips, shunts, stimulators, cochlear implants, or
electrodes) or any other metal object within or near the head, excluding the mouth,
that cannot be safely removed

- Implanted neurostimulators

- History of abnormal MRI

- Known or suspected pregnancy

- If participating in psychotherapy, must have been in stable treatment for at least 3
months prior to entry into the study, with no anticipation of change in the frequency
of therapeutic sessions, or the therapeutic focus over the duration of the rTMS trial

- Clinically significant laboratory abnormality, in the opinion of the Investigator
based on CBC and biochemistry

- Women of childbearing potential and not using a medically accepted form of
contraception when engaging in sexual intercourse

- Women: if pregnant, planning on becoming pregnant, or currently nursing