May be they stopped the trial because they had enough good results and they are going to analyze it ,who knows ?so there is plenty scenario to imagine
We can always hope. But if one reads the post from @David Ho they clearly state it's due too poor results. Let's hope they are wrong and that Autifony has different news coming.
I called another site and they said they had a phone call from Autifony and they said to stop recruiting, because they are investigating the data. Well, this is all very strange.
Could be that the trial has ended because they full and are investigating the data.
That would make sense. The data is supposed to be analyzed by December 2015 according to clinicaltrials.gov.
May be it's part of the business secrets they did it to discourage others companys who want to work on the potassium channel.We can always hope. But if one reads the post from @David Ho they clearly state it's due too poor results. Let's hope they are wrong and that Autifony has different news coming.
I also called the Birmingham unit this morning (several hours ago) and the lady I with spoke said the same i.e. they are stopping the trial. Then I asked: "Yes - but are you stopping according to plan, or, because of lack-of-efficacy?" and she replied "According to plan."It's what the Birmingham hospital told me.
I am not very happy about it too, but if we have to wait, we will wait. After i got this i was hospitalised for a week. The doctors tried to find whats the problem with me and the send me to neurology for a brain tumor check. So I was standing outside the neurologist office, pretty stressed and upset and suddenly I realised that I am standing among people in a wheelchairs, half-paralyzed people that barely can move half of their body after a stroke, people in a far worse condition than mine. This is the best therapy i got (ok and vinpocetine intravenious). I could be far worse, so 5 years, 10 years, we can wait, it sucks, but we can wait.Which brings me to my conclusion: we will have to endure for at least another 5-10 years at minimum. And that is a scary thought!
So how come he got this email and Danny Boy phoned the hospitals and they said different stuff- sounds like a completely unprofessional lot to me................so ATEOS got a different reply.......I dont understand why David would get such a categoric reply stating that the drug had not been working.....ATEOS obviously now knows something.....and if a message is about to be posted then it means that the trial has failed.............David Ho said:I heard back from the hospital. I take the liberty to copy here the e-mail verbatim as it was sent to me:
Dear David
Unfortunately it is not just at Addenbrookes that the whole trial is being stopped. I became aware of the information as Autifony contacted us last week and all other sites are stopping, and as you have correctly understood the researchers found the drug had not been working.
I am aware that there was only a few months left however Autifony will be posting a statement on their website this week.
I will keep you in mind for any further trials that may appear in the future and stay in contact.
Let's wait for the official statement. Hopefully we will learn the results and future plans.
I also called the Birmingham unit this morning (several hours ago) and the lady I with spoke said the same i.e. they are stopping the trial. Then I asked: "Yes - but are you stopping according to plan, or, because of lack-of-efficacy?" and she replied "According to plan."
And that's when I called Autifony. And like I said in another post several pages back already, I am not going to relay the conversation in detail - except to mention that the website will be updated very shortly. But... I know what was said in the conversation with Autifony (obviously), and think about it: as a company, would you announce something while the trial is still ongoing. Probably not, so...
In addition, I can mention that the lady at the Birmingham hospital was not the person normally in charge (she said).
Lot of speculation today - despite pleas for the opposite!
the best scerio to imagne is that they stoped the trial quickly and they are going to prépare a fast trackedLot of speculation today - despite pleas for the opposite!
We should wait for an update from Autifony. And that's all I will say in this matter.should we panic or start opening a bottle of champagne???
I am not very happy about it too, but if we have to wait, we will wait. After i got this i was hospitalised for a week. The doctors tried to find whats the problem with me and the send me to neurology for a brain tumor check. So I was standing outside the neurologist office, pretty stressed and upset and suddenly I realised that I am standing among people in a wheelchairs, half-paralyzed people that barely can move half of their body after a stroke, people in a far worse condition than mine. This is the best therapy i got (ok and vinpocetine intravenious). I could be far worse, so 5 years, 10 years, we can wait, it sucks, but we can wait.
But i dont know how bad is your T, so excuse me if this offend you. Mine is moderate, some days mild, sometimes severe.
We should wait for an update from Autifony. And that's all I will say in this matter.
I think the only answer is trobalt now..................or TRT and back to that!Keeps me with deciding to live with it or to experiment with epilepsy drugs.
Listen... I work (unpaid) with researchers in the background - just today my most regular contact confirmed to me that "Trobalt is interesting" (at the moment we are collecting data here on TT with specific volunteers for in-depth analysis - but no one knows as it is not announced). If the following update on the social media from Team Trobalt many months ago had been shared/rated as requested, it is quite possible that we would now be in a different situation. We did within Team Trobalt a massive publicity campaign to get attention for the cause. Hundreds of hours of work... Whether people realize it or not, Team Trobalt has done a fantastic job (and those are not my words, but the words of some of folks who observe what is going on here on TT...!):I would take sitting in a wheelchair over this thing any day. I would let them saw off my legs with a hacksaw if I could get rid of this thing forever. But that's me!
So moving forward ATEOS what is the solution now ?As I see it, the tinnitus community has failed itself, and, has itself to thank for it. And I truly mean that. And this is just the beginning (unfortunately).
Listen... I work (unpaid) with researchers in the background - just today my most regular contact confirmed to me that "Trobalt is interesting" (at the moment we are collecting data here on TT with specific volunteers for in-depth analysis - but no one knows as it is not announced). If the following update on the social media from Team Trobalt many months ago had been shared/rated as requested, it is quite possible that we would now be in a different situation. We did within Team Trobalt a massive publicity campaign to get attention for the cause. Hundreds of hours of work... Whether people realize it or not, Team Trobalt has done a fantastic job (and those are not my words, but the words of some of folks who observe what is going on here on TT...!):
There was a unique opportunity to help spread the word by a simple click of the button. Not asking for financial donations or anything. But... A SIMPLE MOUSE CLICK!!!
As I see it, the tinnitus community has failed itself, and, has itself to thank for it. And I truly mean that. And this is just the beginning (unfortunately).
attheedgeofscience
12/OCT/2015.
I liked the TT thing on fb ages ago and I have TT appear on my fb page.....I think that on Facebook there is a big chance that any news might get lost in someones news feed. I for one surly miss 90% of things on Facebook just because my feed is literately flooded everyday. I for one did not see that post, or many of the posts that was made through Tinnitus Hub.
During the evolution of this thread...I think that on Facebook there is a big chance that any news might get lost in someones news feed. I for one surly miss 90% of things on Facebook just because my feed is literately flooded everyday. I for one did not see that post, or many of the posts that was made through Tinnitus Hub.
I think there is a possibility that not all of the members of TT have found their way to the Facebook page. Heck I bet there are people on this forum who don't even have Facebook or Twitter.
I returned to TT to collect some behind-the-scenes data. And as can be seen from this update...So moving forward ATEOS what is the solution now ?
During the evolution of this thread...
www.tinnitustalk.com/threads/retigabine-trobalt-potiga-%E2%80%94-petition-to-the-ata.6896
...there were at least 5 internal alerts generated for various posts - all of which one way or another linked to the activities of Team Trobalt and the team of professors in the USA. In addition, updates where done in newsletter material that was e-mailed to all members, and I believe there was also a banner put up (but I am not sure any longer). And besides that the updates themselves were announced on both Twitter and Facebook. Trouble is: if the +100k visitors of TT do not sign-up to become members, we cannot engage them (except with a banner that will be visible to everyone).
There is no way you - and others - could not have known... unless you purposely choose to not get involved (e.g. certain members have their internal alerts disabled). For instance, the ATA thread was pinned (so that you would have seen the updates the very minute you click on the "Treatments" section). In addition, members should have paid attention to the Team Trobalt badge that certain members have/had. It means something. But of course +80% of members would rather spend their time debating instead of listening to those very few who are truly well connected with researchers and have a strategy of what to do.
attheedgeofscience
12/OCT/2015.
I am just stating the P L A I N simple facts.I think it's a bit unfair that you are trying to make people feel guilty.
Actually @attheedgeofscience explained quite well how we've alerted people to important posts (site-wide alerts, banners, email newsletters, social media updates); I would say it is pretty much impossible for someone who visited during those times those updates were sent out to have missed out on them.I think it's a bit unfair that you are trying to make people feel guilty.
Actually @attheedgeofscience explained quite well how we've alerted people to important posts (site-wide alerts, banners, email newsletters, social media updates); I would say it is pretty much impossible for someone who visited during those times those updates were sent out to have missed out on them.
It's less than 0.1% of our visitors that are interested in engaging in the aforementioned matters which @attheedgeofscience stated.
Our community is great, no doubt about it. There is a need for support and we fill that space. We have great members offering wonderful support.
But when it comes to this, there is no denying it; the tinnitus community at large seems relatively apathetic.