Status:
COMPLETED
Phase I/II Study of the Safety, Efficacy and Dose Evaluation of ProSavin for the Treatment of Bilateral Idiopathic Parkinson's Disease
Lead Sponsor:
Oxford BioMedica
Conditions:
Parkinson's Disease
Eligibility:
All Genders
48-65 years
Phase:
PHASE1
PHASE2
Brief Summary
The primary objectives of the trial are to assess the safety and efficacy of ProSavin. Patients in the trial will have been diagnosed with Parkinson's disease and will be failing on current treatment...
Eligibility Criteria
Inclusion
- Willing and able to give written Informed Consent
- Diagnosed with bilateral idiopathic PD
- Diagnosis of PD \> five years, using diagnostic criteria from core assessment program for surgical interventional therapies CAPSIT (1999)
- Males/females between 48 and 65 years
- Women must be postmenopausal, with last menstrual period being over two years ago
- Male patients must agree to use at least two methods of contraception for at least 3 months following ProSavin administration if they and their partner is of child-bearing capacity
- Response to L-DOPA where an increase in dose is unacceptable to the patient due to potentiating the fluctuations in motor functions
- Hoehn and Yahr stage 3 and 4
- UPDRS (Part III) of between 20 and 60 in the "OFF" state
- Stable dosing of PD medication, including L-DOPA, for six weeks prior to surgery
- Positive response to dopaminergic therapy as defined by a 50% improvement in UPDRS (Part III) between the "OFF" and "ON" states
- Presence of motor fluctuations
- Willing to have current treatment withdrawn for up to 24 hours prior to surgery therefore being in an "OFF" state for surgery
- Willing to have their L-DOPA dosage reduced/withdrawn at the discretion of the principal investigator (PI) at regular intervals following surgery to allow assessment of ProSavin in the absence of concomitant anti-{Parkinsonian medication
- Affiliated with the French social security health care system (Patients enrolled in France only)
Exclusion
- Major surgery within the 28 days prior to enrolment
- Severe disabling dyskinesias \> or = 51% of the day as defined by the UPDRS (Part IV)
- History of psychosis or current treatment with dopamine blocking agents of any kind
- Severe depression as defined by a BDI score of \>16. Any treatment for depression should be limited to seretonergic therapies and those that do not target the dopaminergic pathways
- Prior treatment with tolcapone within the six months prior to enrollment into the study, due to its ability to modify dopaminergic pathways in the brain
- History of epilepsy or any other co-morbid condition that the Investigator believes presents an unacceptable health risk to the patient in conjunction with the procedures in this protocol
- Life-threatening illness unrelated to PD
- History of stereotactic or other surgery for the treatment of PD
- Premenopausal women
- Alcohol or other substance abuse
- Clinically significant laboratory test abnormalities, including full blood count, chemistry panel, liver function tests, electrocardiogram (ECG), Chest X rays
- Any contraindication for undergoing an MRI scan of the head
- Intercurrent illness or infection 28 days prior to enrolment
- Abnormal MRI findings such as mega cisterna, septum pellucidum, signs of severe cortical or subcortical atrophy, brain tumours, vascular diseases, trauma or arteriovenous malformations (AVM)
- Prior regular exposure to neuroleptic agents
- History of treatment with any agent that may induce PD or PD symptoms within the last three months prior to enrollment
- Contraindications to use of anaesthesia
- Treated with dopaminergic antagonists six months prior to screening
- Concurrent antiretroviral therapy that would inactivate the investigational agent
- History of any investigational agent within 28 days prior to ProSavin administration
- Participation in a prior gene transfer therapy study
- Enrolment in any other clinical study, for any condition, including those relating to PD, throughout the duration of the ProSavin study
- Current of anticipated treatment with anticoagulant therapy or the use of anticoagulation therapy within the four weeks prior to surgery
- Diagnosis of multiple systems atrophy (MSA) following assessment of the autonomic nervous systems function (e.g. blood pressure, difficulty in urinating and sexual activity) and MRI during the screening process
- Administration of subcutaneous rescue remedy apomorphine
- Patient unable to adhere to their prescribed Parkinson's disease treatment regime.
Key Trial Info
Start Date :
January 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2012
Estimated Enrollment :
15 Patients enrolled
Trial Details
Trial ID
NCT00627588
Start Date
January 1 2008
End Date
August 1 2012
Last Update
May 13 2013
Active Locations (2)
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1
Henri Mondor Hospital
Paris, France
2
Addenbrookes Hospital
Cambridge, Cambridgeshire, United Kingdom, CB2 0QQ