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Optical Coherence Tomography: Glatiramer in Clinically Isolated Syndrome or Early Relapsing Remitting Multiple Sclerosis (MS) (OCTIMS)

Primary Purpose

Multiple Sclerosis

Status
Unknown status
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
glatiramer acetate
Sponsored by
Amphia Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring clinically isolated syndrome, relapsing remitting multiple sclerosis, glatiramer acetate, Optical Coherence Tomography

Eligibility Criteria

18 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 18 - 55 years
  • Early relapsing remitting MS, defined as a disease course less than 3 years
  • clinically isolated syndrome , defined as optic neuritis (ON) or other than ON
  • Currently treated with glatiramer (GA) or currently not treated for MS
  • Expanded disability status scale (EDSS) score 0-5
  • Able and willing to provide written informed consent prior to enrolment
  • Willing and able to comply with the protocol requirements for the duration of the study

Exclusion Criteria:

  • Clinical definite multiple sclerosis with a disease course more than 3 years
  • Primary progressive multiple sclerosis
  • Secondary progressive multiple sclerosis
  • Current use of any approved or investigational disease modifying agents for the treatment of MS other than GA.
  • Neuromyelitis Optica (Devic's disease)
  • Any condition that may interfere with the quality of the OCT scan: clouding of the media, i.e. cataract, pupil which are hard to dilate.
  • Contra-indications for Copaxone ® as defined in the Summary of Product Characteristics (SPC) text
  • Hypersensitivity to GA or mannitol
  • Subject's inability to complete the study or if the subject is considered by the investigator to be for any reason, an unsuitable candidate for this study.

Sites / Locations

  • Amphia ZiekenhuisRecruiting
  • Maasland ZiekenhuisRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

glatiramer acetate

no treatment

Arm Description

glatiramer acetate 20 mg s.c. daily for 1 year

No disease modifying treatment allowed

Outcomes

Primary Outcome Measures

Feasibility of OCT measurement in patient with CIS with or without optic neuritis or with early RRMS in the Dutch clinical setting

Secondary Outcome Measures

Mean change in RNFL in both eyes determined by OCT at baseline, month 3, month 6, month 9, month 12
Other ophthalmological parameters

Full Information

First Posted
May 29, 2009
Last Updated
February 9, 2010
Sponsor
Amphia Hospital
Collaborators
Sanofi, TEVA Pharmachemie
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1. Study Identification

Unique Protocol Identification Number
NCT00910598
Brief Title
Optical Coherence Tomography: Glatiramer in Clinically Isolated Syndrome or Early Relapsing Remitting Multiple Sclerosis (MS)
Acronym
OCTIMS
Official Title
A Multicenter Longitudinal Cross-sectional Pilot Study, to Compare RNFL Thickness Measured by OCT After Treatment With Glatiramer or After no Treatment in Patients With CIS With or Without Optic Neuritis or With Early RRMS
Study Type
Interventional

2. Study Status

Record Verification Date
February 2010
Overall Recruitment Status
Unknown status
Study Start Date
September 2009 (undefined)
Primary Completion Date
June 2012 (Anticipated)
Study Completion Date
June 2012 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Amphia Hospital
Collaborators
Sanofi, TEVA Pharmachemie

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a study in patients with clinically isolated syndrome (CIS) and early relapsing remitting multiple sclerosis (RRMS) to assess the effects of glatiramer acetate (GA) subcutaneously on the condition of the optical nerve in comparison to no medicinal therapy during 12 months and to assess the use of Optical Coherence tomography (OCT), a non-invasive ophthalmological technique, in daily practice as an alternative to magnetic resonance imaging (MRI) scanning for follow-up of these patients.
Detailed Description
Multiple sclerosis (MS) is a progressive and demyelinating disease of the central nervous system characterized by inflammation and neurodegeneration. It is characterized by an ongoing process of demyelination and axonal loss, even at the beginning of the disease course, which will result in brain atrophy. A first manifestation of clinical definite MS, is called a clinically isolated syndrome (CIS). Brain atrophy occurs even in patients with a CIS. Optic neuritis (ON) is a common feature of a CIS. The axons in the retina represent the most proximal part of the optic nerve which is devoid of myelin. Because the retina is part of the central nervous system (CNS), measurement of the Retinal Nerve Fiber Layer (RFLN) by Optical Coherence Tomography (OCT) offers the opportunity to visualize the unmyelinated axons of the CNS directly. OCT is a non-invasive method to measure the thickness of the optical layer. The thickness of the RNFL is reduced in MS patients with or without ON history. Glatiramer acetate (GA), an immunomodulatory drug for RRMS and CIS, reduces brain atrophy and stimulates the production of brain-derived neurotrophic factor, which in turn could stimulate neuroregeneration. In this pilot study we would like to assess the feasibility of OCT measurement in patient with CIS other than ON in the Dutch clinical setting and to assess the effect of GA on the RNFL and visual function in patients with CIS or in early relapsing remitting MS patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
clinically isolated syndrome, relapsing remitting multiple sclerosis, glatiramer acetate, Optical Coherence Tomography

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
glatiramer acetate
Arm Type
Experimental
Arm Description
glatiramer acetate 20 mg s.c. daily for 1 year
Arm Title
no treatment
Arm Type
No Intervention
Arm Description
No disease modifying treatment allowed
Intervention Type
Drug
Intervention Name(s)
glatiramer acetate
Other Intervention Name(s)
Copaxone
Intervention Description
20 mg daily s.c. for 1 year
Primary Outcome Measure Information:
Title
Feasibility of OCT measurement in patient with CIS with or without optic neuritis or with early RRMS in the Dutch clinical setting
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Mean change in RNFL in both eyes determined by OCT at baseline, month 3, month 6, month 9, month 12
Time Frame
1 year
Title
Other ophthalmological parameters
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 18 - 55 years Early relapsing remitting MS, defined as a disease course less than 3 years clinically isolated syndrome , defined as optic neuritis (ON) or other than ON Currently treated with glatiramer (GA) or currently not treated for MS Expanded disability status scale (EDSS) score 0-5 Able and willing to provide written informed consent prior to enrolment Willing and able to comply with the protocol requirements for the duration of the study Exclusion Criteria: Clinical definite multiple sclerosis with a disease course more than 3 years Primary progressive multiple sclerosis Secondary progressive multiple sclerosis Current use of any approved or investigational disease modifying agents for the treatment of MS other than GA. Neuromyelitis Optica (Devic's disease) Any condition that may interfere with the quality of the OCT scan: clouding of the media, i.e. cataract, pupil which are hard to dilate. Contra-indications for Copaxone ® as defined in the Summary of Product Characteristics (SPC) text Hypersensitivity to GA or mannitol Subject's inability to complete the study or if the subject is considered by the investigator to be for any reason, an unsuitable candidate for this study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
E.C.A.M. Sanders, MD
Phone
+31 76 5258246
Email
rsc@rsconsultancy.nl
First Name & Middle Initial & Last Name or Official Title & Degree
Raymond J. Schmidt, MD
Phone
+31 575 441001
Email
rsc@rsconsultancy.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
E.C.A.M. Sanders, MD
Organizational Affiliation
Amphia ziekenhuis
Official's Role
Study Chair
Facility Information:
Facility Name
Amphia Ziekenhuis
City
Breda
ZIP/Postal Code
4818 CK
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
E.C.A.M. Sanders, MD
Phone
+31 76 5258246
First Name & Middle Initial & Last Name & Degree
E.C.A.M. Sanders, MD
Facility Name
Maasland Ziekenhuis
City
Sittard
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
R.M.M. Hupperts, MD PhD
Phone
+31 88 4597811
First Name & Middle Initial & Last Name & Degree
R.M.M. Hupperts, MD PhD
First Name & Middle Initial & Last Name & Degree
S.A.M. Knippenberg, MD

12. IPD Sharing Statement

Links:
URL
http://www.amphia.nl
Description
Amphia Hospital Breda Netherlands

Learn more about this trial

Optical Coherence Tomography: Glatiramer in Clinically Isolated Syndrome or Early Relapsing Remitting Multiple Sclerosis (MS)

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