So I went into my neurologist's office earlier today to sign papers for TOUCH as I am starting Tysabri later this month. The nurse there was talking about drugs that are being studied currently and mentioned that he feels Campath should have great benefits for MS.
Has anyone heard of this or been on a study with this medication? If so, what was your experience like?
He said there are only 5 treatments per year and there is no PML risk and no one has died from taking this medicine. I know that it is already out for leukemia, so does that mean it is already safe and should have no problems or differences when used for MS? I'm confused yet so curious about this possible future medication.
Has anyone heard of this or been on a study with this medication? If so, what was your experience like?
He said there are only 5 treatments per year and there is no PML risk and no one has died from taking this medicine. I know that it is already out for leukemia, so does that mean it is already safe and should have no problems or differences when used for MS? I'm confused yet so curious about this possible future medication.
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