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Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy (EPIMSC)

Primary Purpose

Refractory Epilepsy

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
ADRC transplantation in autoimmune refractory epilepsy
Sponsored by
Mossakowski Medical Research Centre Polish Academy of Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory Epilepsy focused on measuring autoimmune epilepsy, refractory epilepsy, ADRC, mezenchymal stem cells, anti-neuronal antibody, Rasmussen encephality, adipose derived regenerative stem cells

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Drug-resistant epilepsy confirmed in anamnesis and diagnostic tests (EEG, MR)
  • Children between 3 and 18 years old
  • Presence of antineuronal antibody in serum or CSF
  • Rasmussen encephalitis (proven cellular immunity pathogenesis)
  • Probable autoimmune pathogenesis (autoimmune diseases in family, febrile infection associated refractory epilepsy)
  • Willing and able to provide written informed consent (patient or legal guardian)

Exclusion Criteria:

  • Refractory epilepsy with proven genetic or metabolic ethiology
  • Neoplastic disease
  • Active inflammatory process at the time of recruitment
  • Coagulation disorder
  • Status epilepticus
  • Participation in another clinical trial
  • Lack of willingness and ability to provide written informed consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Experimental group

    Arm Description

    Autologous ADRC transplantation in autoimmune refractory epilepsy

    Outcomes

    Primary Outcome Measures

    Rate of epileptic seizures
    recording of epileptic seizures frequency, EEG

    Secondary Outcome Measures

    Intelligence test
    The Leiter contains 10 subtests organized into four domains: Fluid Intelligence Visualization, Memory, Attention
    School progress
    teacher references

    Full Information

    First Posted
    September 14, 2018
    Last Updated
    April 14, 2020
    Sponsor
    Mossakowski Medical Research Centre Polish Academy of Sciences
    Collaborators
    Institute of Mother and Child, Warsaw, Poland
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03676569
    Brief Title
    Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy
    Acronym
    EPIMSC
    Official Title
    Intrathecal Autologous Adipose Derived Regenerative Cells Treatment of Autoimmune Determined Refractory Epilepsy - Evaluation of Safety and Efficacy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2020
    Overall Recruitment Status
    Completed
    Study Start Date
    November 15, 2015 (Actual)
    Primary Completion Date
    April 14, 2019 (Actual)
    Study Completion Date
    April 14, 2019 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Mossakowski Medical Research Centre Polish Academy of Sciences
    Collaborators
    Institute of Mother and Child, Warsaw, Poland

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Refractory epilepsies caused by an autoimmune mechanisms lead in children to progressive neurodegeneration. Immunomodulation therapy is effective only in a half of such cases. New approaches are undertaken. It was found that ADRC (adipose derived regenerative cells) isolated from adipose tissue consist mesenchymal stem cells that act as tissue repair cells. The purpose of this experimental study is to evaluate the possibility and safety of the use of multipotent mesenchymal adipose derived regenerative cells (ADRC) in patients diagnosed with an autoimmune determined refractory epilepsy. Study protocol: Intrathecal infusions of autologous ADRC obtained after liposuction followed by isolation by Cytori system will be performed. Procedure will be repeated 3 times every 3 months in each patient. Neurological status, brain MRI, cognitive function and antiepileptic effect will be supervised during 24 months.
    Detailed Description
    Epilepsy is a chronic neurological disorder diagnosed in about 1% of the population, or c. 400,000 patients in Poland. Autoimmune refractory epilepsy is rare but most disabled epilepsy leading to developmental regression. The belief in a positive effect of ADRCs in drug-resistant epilepsy comes from test results showing the ability of mesenchymal cells to concentrate in damaged tissues, as well as their strong immunomodulating, especially anti-inflammatory, properties. Patients with drug resistant epilepsy show decreased numbers of neurons within the epilepsy zone, with most of these being hyperactive and malfunctioning. Additionally, an inflammatory active reaction in affected brain tissue is visible. ADRC-induced activation of endogenous neurogenesis may increase chances that the epilepsy zone will be reduced, and give a positive impact as regards the neuropsychiatric disorders commonly present in patients with epilepsy. Another common process accompanying recurring epilepsy attacks is active inflammation. Per the literature, ADRCs show strong neuroprotective, immunomodulating and antiapoptotic qualities and they may potentially reduce the frequency of epilepsy attacks. Thus, a clinical trial with ADRCs, addressed to drug-resistant epilepsy sufferers would be promising in controlling the epileptic seizures and coexisting behavioral / psychiatric symptoms. The goal is to improve the quality of life of the patients and their caregivers. In patients who were diagnosed with autoimmune drug-resistant epilepsy and have met the set criteria and qualified to take part in the examination, after a formal written consent of their parents at the Clinic of Child Neurology IMC neurological examination, routine laboratory tests, EEG and neuropsychological assessment will be performed. ADRC will be obtained after liposuction and isolation with Cytori system. Before intrathecal transplantation of ADRC suspension ( 5 ml), cerebrospinal fluid will be collected for evaluation of origin protein level, oligoclonal bands, the IgG index as well as GluR3, VGKC complex/LGI1, GM1, NT-3, GAD, and NMDAR antibodies. At the same time there will be an intake of 5ml of serum to evaluate levels of immunoglobulins IgA, IgM and IgG. Procedure will be repeated 3 times every 3 months in each patient. Neurological status, brain MRI, cognitive function and antiepileptic effect will be supervised during 24 months.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Refractory Epilepsy
    Keywords
    autoimmune epilepsy, refractory epilepsy, ADRC, mezenchymal stem cells, anti-neuronal antibody, Rasmussen encephality, adipose derived regenerative stem cells

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 1
    Interventional Study Model
    Single Group Assignment
    Model Description
    Experimental clinical treatment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    6 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Experimental group
    Arm Type
    Experimental
    Arm Description
    Autologous ADRC transplantation in autoimmune refractory epilepsy
    Intervention Type
    Biological
    Intervention Name(s)
    ADRC transplantation in autoimmune refractory epilepsy
    Primary Outcome Measure Information:
    Title
    Rate of epileptic seizures
    Description
    recording of epileptic seizures frequency, EEG
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    Intelligence test
    Description
    The Leiter contains 10 subtests organized into four domains: Fluid Intelligence Visualization, Memory, Attention
    Time Frame
    3 months
    Title
    School progress
    Description
    teacher references
    Time Frame
    3 months
    Other Pre-specified Outcome Measures:
    Title
    Radiological assesment
    Description
    MRI
    Time Frame
    12 months
    Title
    The level of antineural antibodies
    Description
    protein level, oligoclonal bands, IgG index as well as GluR3, VGKC complex/LGI1, GM1, NT-3, GAD, NMDAR antibodies from cerebrospinal fluid for evaluation the origin
    Time Frame
    3 months

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Drug-resistant epilepsy confirmed in anamnesis and diagnostic tests (EEG, MR) Children between 3 and 18 years old Presence of antineuronal antibody in serum or CSF Rasmussen encephalitis (proven cellular immunity pathogenesis) Probable autoimmune pathogenesis (autoimmune diseases in family, febrile infection associated refractory epilepsy) Willing and able to provide written informed consent (patient or legal guardian) Exclusion Criteria: Refractory epilepsy with proven genetic or metabolic ethiology Neoplastic disease Active inflammatory process at the time of recruitment Coagulation disorder Status epilepticus Participation in another clinical trial Lack of willingness and ability to provide written informed consent
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Dorota Antczak-Marach, M.D.
    Organizational Affiliation
    Institute of Mother and Child
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Ewa Sawicka, Prof.
    Organizational Affiliation
    Institute of Mother and Child
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    32190059
    Citation
    Szczepanik E, Mierzewska H, Antczak-Marach D, Figiel-Dabrowska A, Terczynska I, Tryfon J, Krzesniak N, Noszczyk BH, Sawicka E, Domanska-Janik K, Sarnowska A. Intrathecal Infusion of Autologous Adipose-Derived Regenerative Cells in Autoimmune Refractory Epilepsy: Evaluation of Safety and Efficacy. Stem Cells Int. 2020 Jan 3;2020:7104243. doi: 10.1155/2020/7104243. eCollection 2020.
    Results Reference
    result

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    Intrathecal Autologous ADRC Treatment of Autoimmune Refractory Epilepsy

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