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

Stopped early · Not applicable

Conditions studied: Secondary Progressive Multiple Sclerosis

In brief

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.

Key facts

Study ID

NCT02296346

Run by

University of Utah

People needed

13

Starts

2014-10-01

Expected to finish

2018-05-10

Last updated by the study team

2019-08-14

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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

Where it is running

• University of Michigan Health Systems — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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