Pramipexole for Binge Eating Disorder

Inclusion Criteria:

- Male or female

- Age 18-50 years

- Women of child-bearing potential and males must agree to practice an accepted method
of birth control. All women must have a negative pregnancy test at baseline.

- Good general health as demonstrated by history and physical examination.

- Body mass index of 30 kg/m2 or higher at the screening visit.

- Meet criteria for binge eating disorder as assessed through the SCID-1 and EDE.

Exclusion Criteria:

- Subjects with any unstable medical condition, or any current or past medical
condition which in the opinion of the study physician and/or the principal
investigator may increase the risks associated with pramipexole and study
participation. Medical appropriateness will be determined through history and
physical exam.

- Subjects with any current Axis I psychiatric diagnosis as determined through the
Structured Clinical Interview for DSM-IV for Axis I disorders (SCID-1) interview
(aside from BED).

- Subjects with a Hamilton Depression Rating Scale score greater than or equal to 12 at
the screening visit.

- Subjects who report any history of hallucinations or delusions.

- Participants taking an antidepressant or other regularly used psychotropic medication
which may confound the study results

- Subjects with any current or history of an impulse control spectrum disorder, other
than binge eating disorder,(such as pathological gambling, compulsive shopping, etc.)
at screening as determined by the Structured Clinical Interview for DSM-IV Impulse
Control Module.

- Subjects with any history of suicide attempts or current suicidal ideations.

- Subjects that have used tobacco products on a routine basis within the past six
months.

- Subjects enrolled in any formal treatment programs or research protocols for binge
eating disorder at present, or within the past 30 days.

- Subjects routinely taking any medication known to produce weight change (ex.
olanzapine, amitriptyline, steroid medications, etc., other than oral contraceptives,
stable thyroid replacement drugs, etc.), or medications with drug-drug interactions
with pramipexole.

- Subjects who are currently breast-feeding.

- Subjects who have participated in an investigational drug trial in the past 30 days.

- Subjects who meet DSM IV-TR criteria for alcohol or drug abuse in the past year.

- Subjects with an allergy to pramipexole or tablet constituents.

- Subjects with hepatic dysfunction as determined through a hepatic panel obtained at
the screening visit.

- Subjects with an elevated blood pressure or pulse at screening (140/90 mmHg or above
or pulse of greater than 100 beats/minute after being seated and stationary for at
least five minutes, or as determined at the discretion of the study physician and/or
principal investigator) or history of serious cardiac events (myocardial infarction,
arrhythmia, stroke, etc).

- Subjects with a history of renal dysfunction or with a creatinine clearance of less
than 60 ml/min based upon a serum creatinine obtained during screening and as
calculated with the Cockroft and Gault equation.

- Subjects with a positive urine drug screen.

- Any participant with Parkinson's disease or symptoms suggestive of probable
Parkinson's disease.

- Subjects who have an Epworth Sleep Scale (ESS) score of >7 at screening. ESS scores
> 7 have been associated with an increased risk of sleep attacks (Plowman et al.,
2005).

- Any participant who demonstrates clinically significant orthostatic blood pressure
changes or is symptomatic during the screening visit, as defined under "orthostatic
blood pressure monitoring."

- History of bariatric surgery.

- Participants who report a history of obstructive sleep apnea, excessive fatigue, or
any sleep disorder which in the opinion of the principal investigator or study
medical personnel would increase the participant's risk of experiencing excessive
somnolence with pramipexole.

- Participant has had a change in medication regimen in the last month (dose, starting
a new medication, or stopping a medication).

- Participant is employed by, or has an immediate family member employed by NRI.

- Participant has participated in a formal weight loss program in the last month (e.g.
Weight Watchers, Jenny Craig, etc.)