FTY720

carolew · Posted: Tue Jan 23, 2007 6:56 pm Post subject:

I thought about that. I will dip it then drink what was dissolved... just in case it is the real think Laughing

CureOrBust · Posted: Wed Jan 24, 2007 4:05 am Post subject:

When you say "dissolved" I am guessing you mean ALL the contents that were in the capsule. Avicel is a common filler which I would guess is water soluble (its a quick release filler), while the actual drug may not be.

carolew · Posted: Wed Feb 07, 2007 3:02 pm Post subject:

I spoke today to someone else on the same study as myself for the FTY720. She has no side effects at all either and feels like she is taking nothing. So, maybe it is just something that is just easy to take or, she too, is on placebo. Rolling Eyes

Carole

CureOrBust · Posted: Thu Feb 08, 2007 1:43 am Post subject:

assuming all things equall (ie they let the rif-raf mix with the actual drug group of patients...) If 1 in 3 are getting a placebo, the chance of you both getting placebo, using probability, is 1 in 9. Now they are odds I think most people would gamble a fair bit of money on in a casino. So it would stand to reason that chances are that it doesnt have side effects on most people.

carolew · Posted: Thu Feb 08, 2007 9:36 am Post subject:

I like that!

carolew · Posted: Thu Feb 08, 2007 9:36 am Post subject:

I like that !

LeoDaV · Newbie Joined: Oct 13, 2006 Posts: 9

Hi!

I have successfully entered the FTY720 phase III trial here in Amsterdam - The Netherlands.

3 day's ago I received my first dose. I had to stay 6 hours for observation.

I've created a blog where I will write any thing I feel extra Smile

or changes in my MS symptoms. Read all about it here.

So far I'm really pleased wit this oral drug.

Greetz,

J.

carolew · Posted: Sun Mar 18, 2007 10:45 am Post subject:

Great LeoDav, I think I am on placebo because the pill is so easy to take and I am still deteriorating sloooowwwwwly. Hope you are on the real thing. Carole

LeoDaV · Newbie Joined: Oct 13, 2006 Posts: 9

carolew · Posted: Sun Mar 18, 2007 2:40 pm Post subject:

Great for you. Keep us posted, I want to know everything about this drug. Carole

Lyon · Posted: Sun Mar 18, 2007 3:51 pm Post subject:

Hi Carole,

I looked at the clinical trial site but don't have a complete understanding of the terms of this trial.

I see that it's double blind with possibility of placebo, .5 or 1.25 dosage but I don't see any mention of a crossover at any point.

IF you are on the placebo you will be on it for 24 months or have they told you there is a crossover at some point?

Bob
_________________
Wife diagnosed with RRMS in Feb. 2006.

ewizabeth · Posted: Mon Mar 19, 2007 9:25 am Post subject:

Hi all,

My neuro's office is going to be in this trial, but they aren't recruiting yet. I'm thinking this one might be a possibility for me? Although I'm also still considering Avonex and Tysabri. I might be changing jobs in the future and don't know if I'll be able to dedicate a lot of time to going to the doctor on the weekdays. Decisions, decisions... Confused

I also have high blood pressure. Sheesh, so many things to consider.

Carole and Leo,
I hope you both have the real thing and get good results. Smile

_________________
Take care,

Ewizabeth

Previously Avonex, Rebif & Copaxone
RRMS
~Tysabri since 6/04/07~

TonyJegs · Posted: Tue Mar 20, 2007 3:25 am Post subject: Fingolimod (FTY720)

Background Fingolimod (FTY720) is a new oral immunomodulating agent under evaluation for the treatment of relapsing multiple sclerosis.

Methods We randomly assigned 281 patients to receive oral fingolimod, at a dose of 1.25 mg or 5.0 mg, or a placebo once daily, and we followed these patients for 6 months with magnetic resonance imaging (MRI) and clinical evaluations (core study, months 0 to 6). The primary end point was the total number of gadolinium-enhanced lesions recorded on T1-weighted MRI at monthly intervals for 6 months. In an extension study in which the investigators and patients remained unaware of the dose assignments (months 7 to 12), patients who received placebo underwent randomization again to one of the fingolimod doses.

Results A total of 255 patients completed the core study. The median total number of gadolinium-enhanced lesions on MRI was lower with 1.25 mg of fingolimod (1 lesion, P<0.001) and 5.0 mg of fingolimod (3 lesions, P=0.006) than with placebo (5 lesions).
The annualized relapse rate was 0.77 in the placebo group, as compared with 0.35 in the group given 1.25 mg of fingolimod (P=0.009) and 0.36 in the group given 5.0 mg of fingolimod (P=0.01).
For the 227 patients who completed the extension study, the number of gadolinium-enhanced lesions and relapse rates remained low in the groups that received continuous fingolimod, and both measures decreased in patients who switched from placebo to fingolimod.
Adverse events included nasopharyngitis, dyspnea, headache, diarrhea, and nausea. Clinically asymptomatic elevations of alanine aminotransferase levels were more frequent with fingolimod (10 to 12%, vs. 1% in the placebo group).
One case of the posterior reversible encephalopathy syndrome occurred in the 5.0-mg group. Fingolimod was also associated with an initial reduction in the heart rate and a modest decrease in the forced expiratory volume in 1 second.

Conclusions In this proof-of-concept study, fingolimod reduced the number of lesions detected on MRI and clinical disease activity in patients with multiple sclerosis. Evaluation in larger, longer-term studies is warranted.

Fingolimod (FTY720)
Mechanism of Action, Potential Clues:
Sphingosine-1-Phosphate (S1P) blocks egress from lymph nodes rather than enhancing migration to them.
Effects on migration: Prevents lymphocyte egress. Tightens endothelial junctions. Direct effects on lymphocytes.
S1P Preferential depletion of naïve T cells. Adoptively transferred in vitro activated, polarized T cells do not deplete with Fingolimod.

Red Flags:
- New therapy agent based on old autoimmunity of MS.
- In 1 year period the evaluation of numbers of new lesions and relapses must be considered as not accurate as it shows, means- it proves nothing. Natural Course of MS must be evaluated separately first, and only than you form the group. More, the impressive numbers were shown after 6 months, it is too short.
- There is no information provided on lesions numbers in all groups before trial, so this extrimely valuable information missed.
- We don't know what kind of MS was taken; age of patients, time from onset, etc are also unknown.
-I case of encephalopathy in less than 200 patients (group1 and 2) and in in a period less than 6 months?

Kind regards,
Tony

Lyon · Posted: Tue Mar 20, 2007 7:03 am Post subject:

Hi Tony,
I'm having a hard time discerning what you've copied and pasted from an article and your comments. Your only comments start with the words "Red Flags"?

Thanks,
Bob
_________________
Wife diagnosed with RRMS in Feb. 2006.

TonyJegs · Posted: Tue Mar 20, 2007 6:28 pm Post subject: