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Completed

NCT Number: NCT01719159

Intrathecal Therapy With Monoclonal Antibodies in Progressive Multiple Sclerosis

This is a is a small scale open phase two interventional study to assess long-term stabilising effects of on neurological symptoms by regular intrathecal administered monoclonal antibodies in progressive multiple sclerosis.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of neurology, Umeå University Hospital, Umeå, Sweden

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About this study

There is presently no efficient therapy available in progressive MS, especially if there is no clear evidence of active inflammatory lesions or exacerbations as part of the disease. There are, however, evidence that some treatment protocols using cytotoxic drugs may to some extent slow down the progressive course. One specific feature of long-standing MS is that inflammatory cells accumulate in the central nervous system(CNS) compartment in the subarachnoid and perivascular spaces and may therefore be hard to reach via standard drug delivery through systemic administration. Administration of substances via the Intrathecal (IT) route, however, have shown to efficiently distribute in the subarachnoid spaces and may therefore be an attractive route of drug delivery

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Between the age of 18 and 65 years of age (nonfertile women or fertile women with effective contraceptive methods)
  • Progressive MS since at least three years
  • Some kind of documented progression of neurological symptoms during the previous two years.
  • Expanded Disability Status Scale (EDSS) 4,0 - 7.0 (inclusive) (basically spared arm functions)
  • Conventional therapy not indicated, contraindicated or failed
  • Judged as compliant with the protocol

Exclusion criteria

  • Eligible for any of the conventional MS therapies
  • Relapsing remitting multiple sclerosis (RRMS)
  • Bleeding diathesis or medication contraindicating neurosurgical procedures or lumbar puncture
  • Cognitive defect making informed consent unreliable
  • Any medical condition contraindicating minor surgical procedures, as judged by anaesthesiologist
  • Severe, uncontrolled heart disease
  • Pregnant or lactating women
  • Patients having contraindication for or otherwise not compliant with MRI investigations
  • Documented vulnerability to infections
  • Simultaneous treatment with other immunosuppressive drugs
  • Documented allergy or intolerance to Rituximab
  • Severe psychiatric condition

Treatment and study plan

Rituximab

Drug

25 mg rituximab is injected intrathecally via an Ommaya reservoir once a week for 3 weeks. Patients are then followed for one year.

Other names: Mabthera

Primary outcomes

  1. Number of participants with adverse events

    Time frame: One year after completed treatment

    Feasibility of IT administered monoclonal antibodies

Secondary outcomes

  1. Stabilisation of the neurological deterioration

    Time frame: At 3,6,9,12 month after completed treatment

    Questionaires regarding MS quality of life, symptom inventory and fatigue will be used.

Other outcomes

  1. Immunological markers in blood

    Time frame: At 3,6,9,12 month after treatment

    I.e. absolute numbers of major lymphocyte subset as well as regulatory cell subset

  2. Immunological markers in cerebrospinal fluid (CSF)

    Time frame: At 3, 6, 9 12 month after treatment

    I.e. absolute numbers of major lymphocyte subset as well as regulatory cell subset

Sponsors and collaborators

Lead sponsor

Anders Svenningsson

Other

Collaborators

  • Västerbotten County Council, Sweden

Registry information

Acronym: ITT-PMS

Important dates

Study start
2009
Primary completion
2016
Study completion
2016
First posted
Nov 1, 2012
Registry last updated
Nov 22, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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