Working...
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 94 of 2152 for:    MULTIPLE SCLEROSIS

Open-Label Study to Evaluate the Efficacy of ECP in Secondary Progressive Multiple Sclerosis (MSECP)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02296346
Recruitment Status : Suspended (PI Changed sites and we are waiting to open it at the new site.)
First Posted : November 20, 2014
Last Update Posted : May 17, 2016
Sponsor:
Collaborator:
Mallinckrodt
Information provided by (Responsible Party):
Benjamin M. Segal, M.D., University of Michigan

Brief Summary:
In this research study, the investigators will determine whether a procedure called Extracorporeal Photopheresis (ECP) is helpful in preventing progression of disability in people with SPMS when compared to monthly corticosteroid infusions. This study will determine whether ECP has an effect on inflammatory cells in people with SPMS and whether it has a beneficial therapeutic effect.

Condition or disease Intervention/treatment Phase
Secondary Progressive Multiple Sclerosis Drug: SoluMedrol Device: Extracorporeal Photopheresis Phase 1

Detailed Description:

This is a Phase II randomized, open-label study to evaluate the efficacy of extracorporeal photopheresis (ECP) versus IVMP on disability progression in subjects with SPMS. At the initial screening visit, an extensive medical history will be obtained and a detailed neurological examination will be performed to determine eligibility. Subjects who meet eligibility criteria will be enrolled in one of two study arms. Subjects will be randomized at a 1:1 ratio to receive ECP (study arm) or active treatment with intravenous methylprednisolone pulses (control arm) administered every 4 Weeks (1 gram per infusion) for 52 weeks.

ECP will be administered according to the following schedule:

Study Arm: Weeks 1-8: 3 times per week Weeks 9-16: Twice per week Weeks 17-36: Treatment on two consecutive days every 2 weeks (or optionally, one treatment per week) Weeks 37-43: Once every 2 weeks Weeks 44-52: Once every 4 Weeks

All subjects, including patients who receive corticosteroids, will be evaluated using the MSFC tool at baseline and every 3 months through 2 years. They will also be scored using the EDSS at baseline and every 3 months through 2 years. Subjects in the control arm will be evaluated by MSFC and EDSS during the week prior to their next intravenous methylprednisolone infusion and every three months from baseline through two year mark. Blood will be collected for immune function (cytokines) testing at baseline, and months 3, 6, 9 and 12. MRI will be done at baseline as well as months 6 and 12 following initiation of treatment; if the disability measurements are stable or improved at any point in time, then ECP will be continued per protocol..

Patients in the ECP arm should have all of their treatments with the CELLEX ® System. Patients randomized to the ECP arm must receive their treatment within 5 days of baseline visit.

In the ECP process, UVADEX ® (methoxsalen) Sterile Solution will be injected directly the recirculation bag of the extracorporeal circuit after completion of the buffy coat collection. The dose of UVADEX® (methoxsalen) Sterile Solution will be calculated based on the standard treatment volume formula.


Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 66 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Randomized, Controlled, Open-Label Study to Evaluate the Efficacy of Extracorporeal Photopheresis (ECP) Versus Corticosteroids in the Treatment of Patients With Secondary Progressive Multiple Sclerosis (SPMS)
Study Start Date : October 2014
Estimated Primary Completion Date : October 2017

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Active Comparator: Corticosteriod arm
Patients will receive 1 gram of IV SoluMedrol over 1 hour, once every month for 12 months.
Drug: SoluMedrol
Infusion of drug subcutaneously, once a month.
Other Name: Corticosteriods

Experimental: Extracorporeal Photopheresis

Patient will receive an Extracorporeal Photopheresis treatment at a set frequency over the course of 1 year. The treatment takes about 2-3 hours per session to complete. The treatment schedule is as follows:

ECP will be administered according to the following schedule:

Study Arm: Weeks 1-8: 3 times per week Weeks 9-16: Twice per week Weeks 17-36: Treatment on two consecutive days every 2 weeks (or optionally, one treatment per week) Weeks 37-43: Once every 2 weeks Weeks 44-52: Once every 4 Weeks

Device: Extracorporeal Photopheresis
This intervention is the placement of up to two IV's to extract your blood as a set volume, separate out the white cells and return the red cells to your body. Then the white cells are treated with a drug called UVADEX (methoxsalen), excited by a UV light and returned to your body. Once IV is to withdraw your blood and the other is to return your blood to your body.
Other Names:
  • ECP
  • Cellex machine
  • Therakos




Primary Outcome Measures :
  1. To evaluate the effect of ECP compared to IVMP on accumulation of disability (composite of components of MSFC score) at 1 year (52 weeks) in individuals with secondary progressive multiple sclerosis (SPMS [ Time Frame: 1 year ]
    To evaluate the effect of ECP compared to IVMP on accumulation of disability at 1 year (52 weeks) in individuals with secondary progressive multiple sclerosis (SPMS). Disability will be assessed using a composite measure that takes into account changes in the EDSS and components of the MSFC score.


Secondary Outcome Measures :
  1. Immunological parameters in relation to SPMS [ Time Frame: 2 year ]
    • To determine whether changes in immunological parameters that occur following initiation of ECP or corticosteroids correlate with clinical outcomes



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with SPMS based on the Recommended Diagnostic Criteria for MS and clinical course.
  • Demonstrate EDSS scores between 3 to 6.5 at screening.
  • Documented EDSS progression in the 2 years prior to screening of 1 point or greater for patients with an EDSS score less than 6 at baseline, and greater than or equal to 0.5
  • Documented absence of clinical relapse within 2 years of screening
  • Age ≥ 18 ≤ 75 years
  • Weight > 40≤ 150 kg.
  • Absolute Neutrophil count ≥ 2,000 per μL
  • Hematocrit ≥ 28 % and platelet count > 100,000 per μL (with or without transfusion support)
  • Willingness to use at least 1 reliable method of birth control (e.g. abstinence, oral contraceptives, intrauterine devices, barrier method with spermicide, or surgical sterilization) throughout the study for all men and women of childbearing potential
  • Willingness to participate in all study visits and procedures, as outlined in the informed consent
  • Patients able to give informed consent.
  • Patients must have adequate peripheral venous access to initiate ECP therapy.

Exclusion Criteria:

  • Absolute medical contraindication to corticosteroid treatment
  • Absolute medical contraindication to receive ECP
  • Clinical relapse within 2 years of screening
  • Laboratory evidence of any of the following:

    • WBC < 2,000 cells per uL
    • Serum transaminase levels > x 2 UNL
    • HgbA1C > 6%
  • Concurrent diagnosis of a neurological condition or autoimmune disease other than MS
  • Evidence of known infection with human immunodeficiency virus (HIV) or active (not including latent) Hepatitis B (laboratory testing is not required if virus status is already known)
  • Uncontrolled infection requiring treatment at study entry
  • Hypersensitivity or allergy to psoralen (methoxsalen)
  • Hypersensitivity or allergy to both heparin and citrate products (If hypersensitive or allergic to only one of these products, exclusion does not apply)
  • Inability to tolerate fluid changes associated with ECP (e.g. inadequate renal, hepatic, pulmonary and cardiac function leading to enable patient to tolerate extracorporeal volume shifts associated with ECP)
  • Presence of aphakia or photosensitive disease (systemic lupus erythematosis, porphyrias, albinism, etc.)
  • Women who are pregnant and/or lactating.
  • Use of any investigational drug/treatment at the time of enrollment or within the previous 60 days, or five elimination half-lives, or until the expected pharmacodynamic effect has returned to baseline, whichever is longer.
  • Initiation of dalfampridine or change in the dose of dalfampridine within 6 months prior to randomization
  • Treatment with any of the medications or procedures listed below:

    • Glatiramer acetate, interferon-beta, fingolimod, teriflunomide or dimethylfumarate within 3 months prior to randomization
    • Natalizumab within 6 months prior to randomization
    • Cyclophosphamide within 1year prior to randomization
    • Mitoxantrone within 2 years prior to randomization
    • Rituximab, ofatumumab, ocrelizumab, cladribine, daclizumab within 2 years prior
    • Intravenous immunoglobulin within 6 months prior to randomization
    • Plasmapheresis within 1 year prior to randomization
    • Corticosteroids within 3 months prior to screening
  • Inability to undergo MRI scans
  • Contraindication to gadolinium due to past allergic, hypersensitive or adverse reaction or impaired renal function
  • Any other disease or condition which, in the opinion of the investigator, could interfere with participation in the study according to the study protocol, or with the ability of the patients to cooperate and comply with study procedures.
  • Poor venous access
  • Previous history of skin cancer, leukemia/lymphoma/myeloma or bone marrow transplant.
  • History of cataracts
  • Patients taking Coumadin who are unable to switch from oral anticoagulants to enoxaparin.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02296346


Locations
Layout table for location information
United States, Michigan
University of Michigan Health Systems
Ann Arbor, Michigan, United States, 48109
Sponsors and Collaborators
University of Michigan
Mallinckrodt
Investigators
Layout table for investigator information
Principal Investigator: Benjamin Segal, MD University of Michigan, Director of Multiple Sclerosis Center
Principal Investigator: Daniel Couriel, MD University of Utah, Huntsman Cancer Institute, Internal Medicine

Layout table for additonal information
Responsible Party: Benjamin M. Segal, M.D., Director of the Multiple Sclerosis Center, University of Michigan
ClinicalTrials.gov Identifier: NCT02296346     History of Changes
Other Study ID Numbers: HUM00083301
First Posted: November 20, 2014    Key Record Dates
Last Update Posted: May 17, 2016
Last Verified: May 2016

Additional relevant MeSH terms:
Layout table for MeSH terms
Sclerosis
Multiple Sclerosis
Multiple Sclerosis, Chronic Progressive
Neoplasm Metastasis
Pathologic Processes
Demyelinating Autoimmune Diseases, CNS
Autoimmune Diseases of the Nervous System
Nervous System Diseases
Demyelinating Diseases
Autoimmune Diseases
Immune System Diseases
Neoplastic Processes
Neoplasms
Methylprednisolone Hemisuccinate
Methylprednisolone Acetate
Methylprednisolone
Prednisolone
Prednisolone acetate
Prednisolone hemisuccinate
Prednisolone phosphate
Anti-Inflammatory Agents
Glucocorticoids
Hormones
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Neuroprotective Agents
Protective Agents
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Antiemetics