Autologous Bone Marrow Derived Stem Cells for the Treatment of Multiple Sclerosis.

NCT ID: NCT03069170

Last Updated: 2020-03-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-31

Study Completion Date

2021-01-31

Brief Summary

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Until now, there is no effective approach to stop the progression of multiple sclerosis and stimulate re-myelination. Autologous stem cell transplantation shows hope and is quickly developing as an alternative therapy. We propose the use of autologous bone marrow-derived specific stem cell populations and mesenchymal stem cell transplantation (BM-MSC) associated with immuno-modulation to treat patients with relapsing-remitting MS (RRMS).

Detailed Description

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Multiple sclerosis (MS) is an autoimmune de-myelinating disease in which the myelin sheaths of nerve cells in the central nervous system are damaged.This damage disrupts the ability of parts of the nervous system to communicate, resulting in a range of signs and symptoms, including physical, mental, and psychiatric issues. To date, There is no known cure for multiple sclerosis. Treatments attempt to improve function after an attack and prevent new attacks.

Stem cells possess strong immunomodulatory properties that are shown to play a role in the maintenance of peripheral tolerance and in the control of autoimmunity and that may stimulate repair and regeneration of lesion. Clinical studies have shown that stem cells can be safely harvested and do not form tumors. Most of human stem cell trials have focused on clinical applications for haematopoietic stem cells (HSC), mesenchymal stem cells (MSC), or both. When administered intravenously they have an immune inhibitory effect that can ameliorate animal autoimmune diseases. MSC transplantation significantly improves clinical outcome in experimental allergic encephalitis (EAE). When administered intravenously, MSC may migrate to inflammatory brain lesions and promote survival of nervous cells. Hence, MSC have become the focus of studies as a potential cell therapy for stimulating neuro-protection in human neurodegenerative diseases such as MS.

We propose a safety and efficacy trial of a intravenous and intrathecal injections of autologous bone marrow-derived stem cells into patients with MS.

Conditions

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Multiple Sclerosis

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Stem Cells

Intravenous administration of purified autologous bone marrow-derived stem cells.

Group Type EXPERIMENTAL

Stem Cell Transplantation

Intervention Type BIOLOGICAL

Intravenous and Intrathecal injections of purified autologus bone marrow-derived stem cells.

Stem Cell Transplantation

Intrathecal administration of purified autolgous bone-marrow derived stem cells.

Group Type EXPERIMENTAL

Stem Cell Transplantation

Intervention Type BIOLOGICAL

Intravenous and Intrathecal injections of purified autologus bone marrow-derived stem cells.

Interventions

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Stem Cell Transplantation

Intravenous and Intrathecal injections of purified autologus bone marrow-derived stem cells.

Intervention Type BIOLOGICAL

Eligibility Criteria

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Inclusion Criteria

* Relapsing-remitting MS (RRMS) patients
* Age 18-50 years
* Disease duration \>= 2 and \<= 10 years
* EDSS: 3.0 - 6.5

* SPMS or PPMSTreatment with any immunosuppressive therapy
* Treatment with interferon-beta or glatiramer acetate within the 30 days prior to transplantation
* Treatment with corticosteroids within the 30 days prior to transplantation
* Relapse occurred during the 60 days prior to transplantation
* History of cancer or clinical or laboratory results indicative of severe systemic diseases, including infection for HIV, Hepatitis B or C
* Pregnancy or risk of pregnancy/ lactation
* Current treatment with an investigational therapy
* Inability to give written informed consent in accordance with research ethics board guidelines
Minimum Eligible Age

20 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stem Cells Arabia

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Stem Cells Arabia

Amman, , Jordan

Site Status RECRUITING

Countries

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Jordan

Central Contacts

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Adeeb AlZoubi, PhD

Role: CONTACT

00962795337575

Facility Contacts

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Adeeb AlZoubi, PhD

Role: primary

00962795337575

Other Identifiers

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SCA-MS1

Identifier Type: -

Identifier Source: org_study_id

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