Multiple Sclerosis Clinical Trial
Comparison of Campath and Rebif Treatment on Cognition in Multiple Sclerosis (MS)
Summary
People with multiple sclerosis (MS) often experience problems with cognitive functioning, which can be debilitating and interfere with their daily functioning. However, research has shown that MS disease modifying agents have had some success in treating cognitive problems. The main purpose of this research study is to investigate how well two medicines (alemtuzumab (Campath®) and interferon beta-1a (Rebif®)) work in treating MS-related cognitive problems (e.g., attention, memory, speed of thinking). Participants enrolled will be assessed prior to their first study-related medication dose and re-assessed throughout treatment. It is expected that participants taking Campath® will demonstrate relative stability in cognitive functioning relative to those taking Rebif®. Specifically, the cognitive performance of Rebif® participants will decline somewhat over time, but the cognitive performance of Campath® participants will remain stable.
Full Description
The current will use a neuropsychological evaluation capable of detecting the broad range of cognitive difficulties associated with relapsing remitting MS (RRMS). It is a sub-study of an investigation already underway, called Care-MS II, in which participants diagnosed with RRMS are treated with either Campath® or Rebif®. We will observe those participants already assigned to one of the two study arms in Care-MS II and compare cognitive functioning over time of those taking Campath® and those taking Rebif®. We will also compare the change in cognitive functioning for each active group to that of a matched control group. This will help to control for practice effects and help to establish whether either medication helps to truly stabilize cognitive decline (i.e., relative to non-MS controls). We will obtain neurocognitive data at baseline (prior to the first study dose of Campath® or Rebif®), 12 months (before second dose for Campath® participants), 14 months (2 months after the second dose for Campath® participants), 24 months (prior to the third dose for Campath® participants), and 26 months (2 months after the third dose for Campath® participants). The neurocognitive battery will include gold-standard traditional neuropsychology measures as well as newer, validated computerized measures capable of detecting changes in attention and processing speed that are often missed by traditional measures. Since participants in Care-MS II will also have MRI data at baseline, 1 year, and 2 years, cognitive findings will be correlated with MRI data and analyzed in a post-hoc, exploratory manner for the participants with MS.
Hypotheses include:
1: Participants taking Campath® will demonstrate relative stability in cognitive functioning relative to those taking Rebif®. Specifically, the cognitive performance of Rebif® participants will decline somewhat over time, but the cognitive performance of Campath® participants will remain stable.
2: Participants taking Campath® will demonstrate similar cognitive change (i.e., change in scores over 2 years) as normal, matched controls.
3: Participants taking Rebif® will demonstrate greater cognitive change (i.e., change in scores over 2 years) as compared to normal, matched controls.
4: Cognitive stability in Campath® participants will correlate with stability in MRI parameters.
5: Cognitive change in Rebif® participants will correlate with greater activity on MRI parameters.
Eligibility Criteria
Inclusion Criteria:
Diagnosis of relapsing remitting MS and enrollment in Care-MS II trial
Non-MS controls must be neurologically healthy (with respect to conditions that impact CNS functioning).
Participants must be between the ages of 25 and 50.
Corrected vision of subjects must be no worse than 20/50.
Participants must have at least 10 years of education.
Participants must be capable of writing and pressing the buttons on a computer mouse.
Participants must be capable of understanding and following all test instructions.
Exclusion Criteria:
Participants with a history of head injury, seizures, or neurological conditions involving the central nervous system (other than MS for the MS groups).
Participants with upper extremity dysfunction which prohibits them from using a computer mouse.
Participants who are colorblind.
Participants with history of psychosis or other severe mental illness.
Participants with current alcohol/substance abuse.
Participants taking medications with potential adverse CNS effects
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There are 7 Locations for this study
Berkely California, 94705, United States
Lexington Kentucky, 40513, United States
Springfield Massachusetts, 01104, United States
Lebanon New Hampshire, 03756, United States
Latham New York, 12110, United States
Rochester New York, 14642, United States
Vienna Virginia, 22180, United States
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