Welcome to This Is MS!

     Modules
· Home
· Content
· Downloads
· Encyclopedia
· FAQ
· Feedback
· Forums
· Journal
· Private Messages
· Recommend Us
· Search
· Site_Map
· Stories Archive
· Submit News
· Surveys
· Top 10
· Topics
· Web Links
· Your Account

     Google
Google
Web
This is MS
These ads help pay for the upkeep of our site. They are automatically served by Google and are not affiliated with This is MS.

     Languages
Select Interface Language:


     Who's Online
There are currently, 35 guest(s) and 3 member(s) that are online.

You are Anonymous user. You can register for free by clicking here

     Next Step

From the creators of This is MS comes Experience Project

EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at Experience Project.

Get started by sharing your Multiple Sclerosis story.


     Donations

To remain unbiased, This is MS does not accept corporate sponsorships.

Therefore, we must rely on our users to help support us. Please donate to our upkeep if you have the means. Thank you!


ThisIsMS.com :: View topic - MBP8298 for the treatment of secondary progressive multiple
 Forum FAQForum FAQ   SearchSearch   UsergroupsUsergroups   ProfileProfile   Log in to check your private messagesLog in to check your private messages   Log inLog in 


MBP8298 for the treatment of secondary progressive multiple

 
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Drug Pipeline
View previous topic :: View next topic  
Author Message
beyondms
Family Member


Joined: Nov 12, 2006
Posts: 56

PostPosted: Thu Jan 18, 2007 4:57 pm    Post subject: MBP8298 for the treatment of secondary progressive multiple Reply with quote

Today, I was offered the opportunity to enroll in the BioMS study looking at the effects of MBP8298 for the treatment of secondary progressive multiple sclerosis. Given that I have slowly but surely progressed in the last few years, I see little options. Let me know what you think.

thanks,

beyondms
Back to top
View user's profile Send private message
dignan
Family Elder


Joined: Aug 12, 2004
Posts: 1212

PostPosted: Thu Jan 18, 2007 8:25 pm    Post subject: Reply with quote

I like the sounds of it because it's an injection every six months, and so far, they don't seem to have experienced any scary side-effects. Have you already been tested to see if you have the right haplotype?
Back to top
View user's profile Send private message
mjs
Family Member


Joined: Jan 18, 2007
Posts: 40

PostPosted: Thu Jan 18, 2007 11:42 pm    Post subject: Reply with quote

Googling this drug only brings up good news. The mechanism of this drug also makes it more appealing in some ways (ie, not a general immunosuppressant). Good luck making your decision!
Back to top
View user's profile Send private message
beyondms
Family Member


Joined: Nov 12, 2006
Posts: 56

PostPosted: Sat Jan 20, 2007 9:13 am    Post subject: Reply with quote

dignan wrote:
I like the sounds of it because it's an injection every six months, and so far, they don't seem to have experienced any scary side-effects. Have you already been tested to see if you have the right haplotype?


I have taken the blood test and I will find out soon if I am eligible for this drug. There are few options for SPMS but this one seems promising for a subgroup of patients. At the hospital, the nurse told me that two patients got worse, two had an improvement on their EDSS score by 1. The problem is that the nurse does not know who is on the placebo and who isn't. That five year study looks incredible but we need to complete this phase III study before passing judgment on the drug's efficacy for SPMS. Also note that BioMS is enrolling patients with RRMS for a new study. Stay tuned.

beyondMS
Back to top
View user's profile Send private message
Display posts from previous:   
Post new topic   Reply to topic    ThisIsMS.com Forum Index -> Drug Pipeline All times are GMT - 6 Hours
Page 1 of 1

 
Jump to:  
You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum
You cannot vote in polls in this forum





We encourage you to also visit our Multiple Sclerosis story and support community on Experience Project. Experience Project is a vast and powerful community where people connect anonymously through life experiences. It's made by the same people who built This is MS, on the premise that no one life experience-- like having MS-- defines a person. It now covers over 2 million life stories. Find and share yours!

Experience Project: I have Multiple Sclerosis


Anonymous Confessions | Free Dream Interpretations | Ask Any Question
Site Map

This site does not offer medical advice. All treatment decisions should always be made with the full consent of your physician.


All logos and trademarks in this site are property of their respective owners. The comments are property of their posters, quoted articles are © referenced source, all the rest © 2002-8 by thisisMS.com.
PHP-Nuke Copyright © 2005 by Francisco Burzi. This is free software, and you may redistribute it under the GPL. PHP-Nuke comes with absolutely no warranty, for details, see the license.
Page Generation: 0.10 Seconds