ENGLISH ABSTRACT
JOURNAL ARTICLE
REVIEW
Add like
Add dislike
Add to saved papers

[Mitoxantrone for the treatment of patients with multiple sclerosis].

Mitoxantrone was originally developed as an antineoplastic agent. However, it is currently used as an immunosuppressant in the treatment of multiple sclerosis (MS). A series of European studies over a 10-year period have revealed the clinical benefits and tolerability of mitoxantrone. On the basis of the favorable findings reported by the above mentioned studies, the FDA approved the use of mitoxantrone for reducing neurologic disability and/or the frequency of clinical relapses in patients with secondary progressive MS, progressive relapsing MS, or worsening relapsing-remitting MS but not for treating patients with primary progressive MS. The therapeutic modalities available in Japan are very limited. Interferon beta (IFN-beta), which is an immunomodulatory drug, is the only drug approved in Japan for treating MS; however, it is only partially effective or rather ineffective for treating patients with rapidly worsening or fulminant MS. Our pilot studies confirmed the benefits of mitoxantrone in Japanese patients with MS, and in this study, we review its potential appliciation for the treatment of MS by Japanese neurologists.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app