Safety of CERE-120 (AAV2-NTN) in Subjects With Idiopathic Parkinson's Disease

Inclusion criteria

• Diagnosis of bilateral idiopathic Parkinson's Disease of at least 5 years duration since diagnosis with motor fluctuations, despite adequate oral antiparkinsonian therapy.
• Diagnosis of moderate to severe Parkinson's Disease based on clinical rating scales.
• Males or nonpregnant females 35-75 years of age, inclusive.
• Stable medication requirements, and clear response to antiparkinsonian medications during the 60-day eligibility evaluation period.
• No conditions that would render the subject unsuitable for surgery, or that would interfere with any of the assessments of safety or efficacy in this trial.
• Subject's informed consent prior to the performance of any study-specific procedure.

Exclusion criteria

• A history of any clinically significant medical, psychiatric, or laboratory abnormality for which participation in the study would pose a safety risk to the subject.
• History of treatment of Parkinson's disease by any procedure involving intracranial surgery or implantation of a device.
• MRI of the brain within 12 months before the anticipated dosing procedure that indicates the presence of an abnormality that may interfere with the assessments of safety or efficacy or would, in the judgment of the investigator, present a surgical risk to the subject.
• Any disorder that precludes a surgical procedure or alters wound healing.
• A score of less than or equal to 25 on the Folstein Mini-Mental examination performed during the eligibility evaluation period.
• Chemotherapy, cytotoxic therapy, or immunotherapy within 6 weeks prior to CERE-120 administration.
• Vaccinations within 30 days prior to CERE-120 administration.
• History, within two years before the anticipated dosing procedure, of drug or alcohol abuse.
• Treatment with nonantiparkinsonian agents that may affect symptoms of Parkinson's disease within 60 days before the anticipated dosing procedure.
• Any medical disability that would interfere with the assessment of safety and efficacy in this trial or would compromise the ability of the subject to undergo study procedures (e.g. MRI, PET) or to give informed consent.
• History of prior gene transfer therapy.
• Treatment with an investigational agent within 60 days before the anticipated dosing procedure.