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Safety Study of Erythropoietin (EPO) in Parkinson's Disease

Primary Purpose

Parkinson Disease

Status
Completed
Phase
Phase 1
Locations
Cuba
Study Type
Interventional
Intervention
Erythropoietin human recombinant (EPOrh)
Sponsored by
International Center for Neurological Restoration, Cuba
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Parkinson Disease focused on measuring Neuroprotection, Parkinson Disease, Erythropoietin

Eligibility Criteria

45 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Hohen and Yahr´s Scale between I and III
  • One or more years of evolution of PD,
  • Good response to levodopa (more that 30 % of change)valued in motor UPDRS
  • An acceptable general health status,

Exclusion Criteria:

  • Chronic psychiatric or other neurological diseases.
  • Previous polyglobulin
  • Hematocryte, same or inferior to 50

Sites / Locations

  • Clinic of Movement Disorders, International Center for Neurological Restoration

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Erythropoietin

Arm Description

There are evidences of neuroprotecting therapeutic alternatives in such substances as erythropoietin (EPO) which is a well-known cytokine as a hematopoietic growth factor, so, it is therefore important to control tissular oxygenation. It is considered that EPO protects the neurons by a combination of several mechanisms. EPOrh is used with high effectiveness in the treatment of anemias with deficiency of erythropoietin.

Outcomes

Primary Outcome Measures

safety assessment measured by the absence of adverse events

Secondary Outcome Measures

Post-treatment change in the motor score of the Unified Assessment Scale for Parkinson Disease´s (UPDRS) in the "OFF" condition as compared with the baseline.

Full Information

First Posted
November 8, 2009
Last Updated
September 27, 2019
Sponsor
International Center for Neurological Restoration, Cuba
Collaborators
Centro de Immunologia Molecular, Cuba
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1. Study Identification

Unique Protocol Identification Number
NCT01010802
Brief Title
Safety Study of Erythropoietin (EPO) in Parkinson's Disease
Official Title
Phase 1 Study of Recombinant Human Erythropoietin (rhEPO) in Parkinson's Disease (PD)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2019
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
International Center for Neurological Restoration, Cuba
Collaborators
Centro de Immunologia Molecular, Cuba

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether recombinant human Erythropoietin (EPOrh) is safe in the treatment of patients with Parkinson's Disease.
Detailed Description
After onset of Parkinson's Disease (PD)- in spite of the use of medications that constitute the symptomatic treatment- the disease is worsens with an inevitable progression, thus causing complications that lead to the loss of patient´s manual skills and independent gait. At present, the treatment of PD with the use of medications is based on dopamine precursors and dopaminergic agonists but as the disease advances, other symptoms that do not respond to dopaminergic stimulation do appear. For this reason, it is a priority to find a way to focus on neuroprotection during the course of the disease. There are evidences of neuroprotecting therapeutic alternatives in such substances as erythropoietin (EPO). Positive results on the neuroprotective/neurotrophic efficacy of EPO in neurological and psychiatric diseases have been obtained from treatment trials, but nevertheless, it is indispensable demonstrate that with the proposed medication doses it's well tolerated by PD patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease
Keywords
Neuroprotection, Parkinson Disease, Erythropoietin

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Erythropoietin
Arm Type
Experimental
Arm Description
There are evidences of neuroprotecting therapeutic alternatives in such substances as erythropoietin (EPO) which is a well-known cytokine as a hematopoietic growth factor, so, it is therefore important to control tissular oxygenation. It is considered that EPO protects the neurons by a combination of several mechanisms. EPOrh is used with high effectiveness in the treatment of anemias with deficiency of erythropoietin.
Intervention Type
Drug
Intervention Name(s)
Erythropoietin human recombinant (EPOrh)
Other Intervention Name(s)
EPOCIM® (Center of Molecular Immunology, Habana, Cuba)
Intervention Description
Administration scheme by subcutaneous via, of an EPOrh solution up to a weekly doses of 60 UI/kg for five weeks
Primary Outcome Measure Information:
Title
safety assessment measured by the absence of adverse events
Time Frame
weeks 1 to 5, 6, 12, 23 and 35
Secondary Outcome Measure Information:
Title
Post-treatment change in the motor score of the Unified Assessment Scale for Parkinson Disease´s (UPDRS) in the "OFF" condition as compared with the baseline.
Time Frame
week 6, 12, 23 and 35

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hohen and Yahr´s Scale between I and III One or more years of evolution of PD, Good response to levodopa (more that 30 % of change)valued in motor UPDRS An acceptable general health status, Exclusion Criteria: Chronic psychiatric or other neurological diseases. Previous polyglobulin Hematocryte, same or inferior to 50
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ivonne Pedroso, M.D., M.Sc.
Organizational Affiliation
International Center for Neurological Restoration
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Lazaro M Alvarez, M.D.
Organizational Affiliation
International Center for Neurological Restoration
Official's Role
Study Director
Facility Information:
Facility Name
Clinic of Movement Disorders, International Center for Neurological Restoration
City
Havana
Country
Cuba

12. IPD Sharing Statement

Citations:
PubMed Identifier
22334107
Citation
Pedroso I, Bringas ML, Aguiar A, Morales L, Alvarez M, Valdes PA, Alvarez L. Use of Cuban recombinant human erythropoietin in Parkinson's disease treatment. MEDICC Rev. 2012 Jan;14(1):11-7. doi: 10.37757/MR2012V14.N1.4.
Results Reference
result
PubMed Identifier
29862060
Citation
Pedroso I, Garcia M, Casabona E, Morales L, Bringas ML, Perez L, Rodriguez T, Sosa I, Ricardo Y, Padron A, Amaro D. Protective Activity of Erythropoyetine in the Cognition of Patients with Parkinson's Disease. Behav Sci (Basel). 2018 May 21;8(5):51. doi: 10.3390/bs8050051. eCollection 2018 May.
Results Reference
result

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Safety Study of Erythropoietin (EPO) in Parkinson's Disease

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