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View topic - Teriflunomide | ThisIsMS.com
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Teriflunomide
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tobi
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Newbie


Joined: Dec 06, 2009
Posts: 5
Location: Brandenburg, Deutschland (Germany)

PostPosted: Sat Dec 12, 2009 10:14 am    Post subject: Reply with quote

here you can look for the different teriflunomide trials:

http://clinicaltrials.gov/ct2/results?term=teriflunomide[/url]
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domheldercamara
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Newbie


Joined: Dec 18, 2009
Posts: 2
Location: Ottawa, Canada

PostPosted: Fri Dec 18, 2009 7:05 pm    Post subject: New to the Site- Thinking of Teriflunomide Clinical Study Reply with quote

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.
Rolling Eyes
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?

Thanks Smile
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DM
Family Member


Joined: Sep 07, 2007
Posts: 97
Location: Ottawa, Canada

PostPosted: Fri Dec 18, 2009 7:14 pm    Post subject: Reply with quote

Dom,

I'm in Ottawa as well. Just finished up the 2 year trial. Now I am on the expanded trial. Except for some thinning of the hair, no sidefx whatsoever.

Don't worry about it. They'll look after you well with frequent visits, ultrasounds, and MRIs.

Guess you are at the General?
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domheldercamara
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Joined: Dec 18, 2009
Posts: 2
Location: Ottawa, Canada

PostPosted: Sun Dec 20, 2009 10:15 pm    Post subject: Teriflunomide Reply with quote

Hey DM,

Thanks for making me less nervous about teriflunomide. I will be at the General with Dr. Christie for the trials.

I am glad to know that there is someone on the forum not only in proximity, but on the same trial.

Thanks again, I think now I will have less trepidation to try this drug out.
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DM
Family Member


Joined: Sep 07, 2007
Posts: 97
Location: Ottawa, Canada

PostPosted: Fri Jan 01, 2010 5:07 pm    Post subject: Reply with quote

It may be the same drug but a different trial. As far as I know, I was the last at the clinic to be in the particular study.
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Jaguar
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Joined: Dec 12, 2009
Posts: 88
Location: Montreal

PostPosted: Wed Jan 06, 2010 12:55 pm    Post subject: Reply with quote

I have been in trials for I think it is now 8 years. Definite hair thinning - happened right at the beginning, then stopped.

But hey, I'm a guy, what can I really expect?
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DM
Family Member


Joined: Sep 07, 2007
Posts: 97
Location: Ottawa, Canada

PostPosted: Wed Jan 06, 2010 1:52 pm    Post subject: Reply with quote

Did it just stop, or start to grow back a bit once the body adjusted to the drug?
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Jaguar
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Joined: Dec 12, 2009
Posts: 88
Location: Montreal

PostPosted: Wed Jan 06, 2010 2:15 pm    Post subject: Reply with quote

No growing back

just thinner and thinner over 4 years or so
now stable
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DM
Family Member


Joined: Sep 07, 2007
Posts: 97
Location: Ottawa, Canada

PostPosted: Thu Jan 07, 2010 9:34 pm    Post subject: Reply with quote

At the rate its going lately, I won't have any left in 2 years, and I did have a lot of hair on my head. I am not happy!
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MartynW
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Joined: Jun 08, 2009
Posts: 8

PostPosted: Fri Jan 22, 2010 9:48 am    Post subject: Bad news Reply with quote

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".

Good news in the paper yesterday

Hope for MS pill after cladribine and fingolimod trials
http://news.bbc.co.uk/1/hi/health/8470138.stm
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sneakypuss_01
Getting to Know You...


Joined: Oct 15, 2009
Posts: 10
Location: Sydney Australia

PostPosted: Mon Apr 19, 2010 5:56 am    Post subject: Reply with quote

Hi All

Just wanted to let you know that I am participating in the phase III trial here in Australia.

I get put into 'randomization' ion May 4th. So far, I am only the second person at my MS Clinic to go into the trial.

Hope everyone is well.
Sneaky P
_________________
There's not brain lesions...their bright ideas.
DX July 1st 2009 RRMS
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sneakypuss_01
Getting to Know You...


Joined: Oct 15, 2009
Posts: 10
Location: Sydney Australia

PostPosted: Wed Apr 21, 2010 12:19 am    Post subject: Reply with quote

For those interested in the trial, here's the offical website:

http://tower3.msstudies.com/index.php
_________________
There's not brain lesions...their bright ideas.
DX July 1st 2009 RRMS
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DM
Family Member


Joined: Sep 07, 2007
Posts: 97
Location: Ottawa, Canada

PostPosted: Wed Apr 21, 2010 3:34 pm    Post subject: Reply with quote

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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sneakypuss_01
Getting to Know You...


Joined: Oct 15, 2009
Posts: 10
Location: Sydney Australia

PostPosted: Tue May 04, 2010 4:51 am    Post subject: Reply with quote

Hey DM

Well, I got given something today...frustrating that we can't know what it is, but I do understand why.

Will definitely keep you posted on my progress.
_________________
There's not brain lesions...their bright ideas.
DX July 1st 2009 RRMS
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