Phase I/II Study of the Safety, Efficacy and Dose Evaluation of ProSavin for the Treatment of Bilateral Idiopathic Parkinson's Disease

Parkinson's Disease Clinical Trial

Official title:

A Phase I/II Study of the Safety, Efficacy and Dose Evaluation of ProSavin®, Administered Using Stereotactic Injection to the Striatum of Patients With Bilateral, Idiopathic Parkinson's Disease.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00627588
• Other study ID #: PS-001-07
• Secondary ID: EudraCT Number:
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: January 31, 2008
• Last updated: May 9, 2013
• Start date: January 2008
• Est. completion date: August 2012

Study information

• Verified date: May 2013
• Source: Oxford BioMedica
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial 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 with L-DOPA but they will not have progressed to drug-induced dyskinesias. The first stage is an open-label dose escalation to evaluate up to three dose levels of ProSavin in cohorts of three patients each. Following a recommendation by the DMC the study may proceed to the second stage of the trial, a further 12 patients will be recruited to confirm efficacy of the optimal dose in the randomized phase of the study.

The efficacy of ProSavin will be assessed using the Unified Parkinson's Disease Rating Score (UPDRS). Patients will be monitored at regular intervals, with the primary endpoint being an efficacy assessment at six months after treatment. The secondary objective of the trial is to asses the extent to which patients' current therapy (L-DOPA) can be reduced following administration of ProSavin.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: August 2012
• Est. primary completion date: August 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 48 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Willing and able to give written Informed Consent

2. Diagnosed with bilateral idiopathic PD

3. Diagnosis of PD > five years, using diagnostic criteria from core assessment program for surgical interventional therapies CAPSIT (1999)

4. Males/females between 48 and 65 years

5. Women must be postmenopausal, with last menstrual period being over two years ago

6. 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

7. Response to L-DOPA where an increase in dose is unacceptable to the patient due to potentiating the fluctuations in motor functions

8. Hoehn and Yahr stage 3 and 4

9. UPDRS (Part III) of between 20 and 60 in the "OFF" state

10. Stable dosing of PD medication, including L-DOPA, for six weeks prior to surgery

11. Positive response to dopaminergic therapy as defined by a 50% improvement in UPDRS (Part III) between the "OFF" and "ON" states

12. Presence of motor fluctuations

13. Willing to have current treatment withdrawn for up to 24 hours prior to surgery therefore being in an "OFF" state for surgery

14. 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

15. Affiliated with the French social security health care system (Patients enrolled in France only)

Exclusion Criteria:

1. Major surgery within the 28 days prior to enrolment

2. Severe disabling dyskinesias > or = 51% of the day as defined by the UPDRS (Part IV)

3. History of psychosis or current treatment with dopamine blocking agents of any kind

4. 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

5. 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

6. 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

7. Life-threatening illness unrelated to PD

8. History of stereotactic or other surgery for the treatment of PD

9. Premenopausal women

10. Alcohol or other substance abuse

11. Clinically significant laboratory test abnormalities, including full blood count, chemistry panel, liver function tests, electrocardiogram (ECG), Chest X rays

12. Any contraindication for undergoing an MRI scan of the head

13. Intercurrent illness or infection 28 days prior to enrolment

14. 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)

15. Prior regular exposure to neuroleptic agents

16. History of treatment with any agent that may induce PD or PD symptoms within the last three months prior to enrollment

17. Contraindications to use of anaesthesia

18. Treated with dopaminergic antagonists six months prior to screening

19. Concurrent antiretroviral therapy that would inactivate the investigational agent

20. History of any investigational agent within 28 days prior to ProSavin administration

21. Participation in a prior gene transfer therapy study

22. Enrolment in any other clinical study, for any condition, including those relating to PD, throughout the duration of the ProSavin study

23. Current of anticipated treatment with anticoagulant therapy or the use of anticoagulation therapy within the four weeks prior to surgery

24. 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

25. Administration of subcutaneous rescue remedy apomorphine

26. Patient unable to adhere to their prescribed Parkinson's disease treatment regime.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Parkinson Disease
• Parkinson's Disease

Intervention

Biological:
• ProSavin
ProSavin is a gene therapy designed to delivery three key enzymes involved in the synthesis of dopamine
• ProSavin
ProSavin is a gene therapy designed to delivery three key enzymes involved in the synthesis of dopamine

Locations

Country	Name	City	State
France	Henri Mondor Hospital	Paris
United Kingdom	Addenbrookes Hospital	Cambridge	Cambridgeshire

Sponsors (1)

Lead Sponsor	Collaborator
Oxford BioMedica

Countries where clinical trial is conducted

France,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety as measured by the number and severity of Adverse Events		1 year	Yes
Secondary	Efficacy as measured by the UPDRS		6 months	Yes