BIIB014 Phase 2a Monotherapy

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00451815
Recruitment Status : Withdrawn
First Posted : March 26, 2007
Last Update Posted : March 26, 2007
Information provided by:

Brief Summary:
To assess the preliminary safety and tolerability of multiple oral doses of BIIB014 in subjects with early PD.

Condition or disease Intervention/treatment Phase
Parkinson's Disease Drug: active drug (BIIB014) at 10, 30, 100, or 300 mg once daily. Drug: placebo Phase 2

Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Treatment
Official Title: A Randomized, Double-Blind, Placebo-Controlled, Dose Escalation Study of Multiple Oral Dose Administration of BIIB014 in Subjects With Early Parkinson’s Disease

Resource links provided by the National Library of Medicine

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   30 Years to 78 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00451815

Sponsors and Collaborators
Study Director: Biogen Idec Biogen Identifier: NCT00451815     History of Changes
Other Study ID Numbers: 204-PD-201
First Posted: March 26, 2007    Key Record Dates
Last Update Posted: March 26, 2007
Last Verified: March 2007

Additional relevant MeSH terms:
Parkinson Disease
Parkinsonian Disorders
Basal Ganglia Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Movement Disorders
Neurodegenerative Diseases
Adenosine A2 Receptor Antagonists
Purinergic P1 Receptor Antagonists
Purinergic Antagonists
Purinergic Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs