have u heard of these med's ( NEW TO THE SITE )

A board to discuss future MS therapies in early stage (Phase I or II) trials.

have u heard of these med's ( NEW TO THE SITE )

Postby baffled » Sat Jan 14, 2012 3:13 pm

:-D
Eveing to all i have a severe reaction to cannulas so i can only take tablet's so i trying to nhs fundind for the new ms drug's which are quite rare in the uk some not

bg12 , leustat, fingolimod, laquinmod, teriflunomide and i also take a parkinson drug for circulation and cramp's roprinole which is fab no side effect's so far

look forward to your thought's :razz: Haze
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Re: have u heard of these med's ( NEW TO THE SITE )

Postby CureOrBust » Sat Jan 14, 2012 5:07 pm

from my understanding, all MS meds you list are on trial except fingolimod, which is sold under the trade name Gilenya; i am actually taking it in Australia.

You may wish to look at the pipeline thread by dignan.
http://www.thisisms.com/forum/drug-pipeline-f13/topic1363.html?hilit=pipeline
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Re: have u heard of these med's ( NEW TO THE SITE )

Postby naychergirl » Mon May 21, 2012 5:26 am

Ihave been taking Gilenya for over a year. Is it any better than doing the shots? I don't think it's really any better, but a least you don't have to do the shots. Prior to the Gilenya, a started out on Copaxone, which did absolutly nothing for me, so I switched to REbif, which worked great and you only had to get shots 3 times a week. My neuro got me into a Gilenya trial, and I've been on it ever since. Still waiting for a cure!
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