| Eligibility |
Inclusion Criteria:
Unless otherwise specified, to be eligible to participate in this study, candidates must
meet the following eligibility criteria at the time of the Baseline Visit (Day -1):
1. Must give written informed consent. Must also provide all authorizations required by
local law.
2. Aged 30 to 78 years old at the time of informed consent.
3. If female, must be postmenopausal for at least 1 year, surgically sterile, or willing
to practice effective contraception during the study. Nursing mothers, pregnant women,
and women planning to become pregnant while on study are to be excluded.
4. Carry a diagnosis of probable idiopathic PD, made by a Movement Disorder Specialist,
with asymmetric onset and at least 2 of the following cardinal features of PD:
bradykinesia, rigidity, or a classic PD resting tremor.
5. Be Hoehn & Yahr Stage I-III inclusive when OFF.
6. Have a Total Unified PD Rating Scale (UPDRS) OFF score of ³ 8.
7. Have taken no prescribed medications for PD for a minimum of 2 weeks before the
Baseline Visit (Day -1).
8. Are willing to abstain from alcohol for the duration of the study.
9. Have no clinically significant baseline ECG (12-lead) and laboratory abnormalities (as
determined by the Investigator), unless exempted by the Biogen Idec Medical Director.
10. Agree to provide blood samples for mRNA and DNA analysis, which will be collected and
banked and may be used for exploratory pharmacogenomic studies.
Exclusion Criteria
Unless otherwise specified, candidates will be excluded from study entry if any of the
following exclusion criteria exist at the time of the Baseline Visit (Day -1):
1. Mini Mental State Examination (MMSE) score <27.
2. History or clinical features such as impaired downward gaze, prominent axial rigidity,
gait initiation failure, autonomic dysfunction, etc. consistent with an atypical
parkinsonism syndrome.
3. Any significant non-PD central nervous system disorder.
4. Significant AXIS I psychiatric disease as defined by Diagnostic and Statistical Manual
of Mental Disorders, 4th edition-Revised (DSM IV-TR, American Psychiatric Association,
2000).
5. History of surgical intervention for PD (pallidotomy, thalamotomy, deep brain
stimulation, etc.).
6. Participation in a previous adenosine A2A trial.
7. Participation in any other investigational drug study within 1 month prior to
randomization into this trial.
8. History of malignancy unless an exemption has been granted by the Biogen Idec Medical
Director.
9. History of severe allergic or anaphylactic reactions to a drug.
10. Clinically significant cardiac, renal, pulmonary, hematopoietic, endocrine, or hepatic
disease.
11. Abnormal laboratory results as follows: AST, ALT, total bilirubin, GGT levels > 1.5 x
upper limit of normal; serum lipase > upper limit of normal; WBC < 4,000 cells/mm3
hemoglobin < 10, or any other abnormal laboratory value that could interfere with the
assessment of safety.
12. Supine (measured in duplicate 10 minutes after resting) or standing (measured in
duplicate 3 minutes after changing from a supine to a standing position) blood
pressure of >150 or <90 mmHg systolic or >90 or <40 mmHg diastolic on 2 consecutive
occasions.
13. Orthostatic hypotension as defined by a decrease in systolic BP of >20 mmHg or in
diastolic blood pressure of > 10 mmHg measured in duplicate 3 minutes after changing
from a supine to standing position.
14. History of human immunodeficiency virus (HIV).
15. Positive for hepatitis C antibody and/or positive for hepatitis B surface antigen
(HBsAg) at screening.
16. History of drug or alcohol abuse as defined by the DSM IV-TR (American Psychiatric
Association, 2000) within 1 year prior to randomization into this trial.
17. Alcohol use within 72 hours of Baseline Visit (Day -1).
18. Donation of blood or plasma in excess of 500 mL within 3 months of the Screening
Visit.
19. Unwillingness or inability to comply with the requirements of the protocol including
the presence of any condition (physical, mental, or social) that is likely to affect
the subject's ability to comply with the protocol.
20. Any other reasons that, in the opinion of the Investigator and/or the Sponsor, the
subject is determined to be unsuitable for enrollment in this study.
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