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Joined: Dec 18, 2009 Posts: 2 Location: Ottawa, Canada
Posted: Fri Dec 18, 2009 7:05 pm Post subject: New to the Site- Thinking of Teriflunomide Clinical Study
My MD asked me if I was interested in participating in the phase III study as I am pretty well petrified of needles...
I am reading the consent form and it says something to the effect that the drug has shown (in test tube studies) alterations to DNA- and can potentially cause cancer..but there is no proof yet in humans.
It makes me equally nervous.
Can anyone speak to the effects the drug has had on them. I understand that hair loss is one of them- its the cancer that really scares me, any words of advice?
Posted: Fri Jan 22, 2010 9:48 am Post subject: Bad news
So, it seems I have 3 new lesions, so am washing out of the drug next week. Oh well, was worth a try. 9 months, no symptoms, perhaps the Placebo, will never know.
Looking into Avonex now.
tbh, its good timing, i was about to go travelling for a year, and the drug company was insist that i travel back to London every 6 weeks for blood tests, which would have been expensive.
Still don't have MS by definition, but as the Doctor says "the ongoing activity is highly suggestive".
I completed the Phase 3 trial this past November. Haven't found out yet what I was taking. On the extended study now, and on the real thing, 7 or 14mg. No noticeable differences except my hair has thinned. No sfx whatsoever. Good luck and let us know how you progress!
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