There is a lot of politics involved.I hope that Frequency Therapeutics did just that. They must have been working on these molecules for many years before coming out with there recent publications.
There is a lot of politics involved.I hope that Frequency Therapeutics did just that. They must have been working on these molecules for many years before coming out with there recent publications.
I don't think any of these gene therapies or stem cell treatments will be deemed suitable for anyone with T or mild to moderate hearing loss. I can't see how they will be able to regrow the specific hair cells that a person with T or mild loss is missing or has damaged. I believe all these treatments will only be available and useful to give some hearing to a profoundly deaf person who uses a cochlear implant so they maybe get use of a hearing aid instead. I'm 39 with T for 10 years now and I expect it to be with me to the end of my life. I wouldn't be building my hopes up for a cure any time soon.
This means that Spiral will complete the "feasibility assessment" by Q3 2017. In simple English, Spiral will see if they can use BN201 and BN119 for the inner ear.
It's not even June yet! Give it more time.We are coming up on the start of Q3 2017. Has anyone heard more from Spiral?
Markethttp://houghear.org/research/ (At the bottom of the text)
their aim is to be able to obtain FDA approval within the next 3-5 years
Is this a product on the market, Or clinical trial?
Yes, BUT they mention the preventive therapy not the regeneration therapyhttp://houghear.org/research/ (At the bottom of the text)
their aim is to be able to obtain FDA approval within the next 3-5 years
Is this a product on the market, Or clinical trial?
Thank you. I should really visit more threads on here.@jeff W, I have posted all the ones I know of in a new thread.
https://www.tinnitustalk.com/threads/companies-developing-cures.21781/
Yes, but there is also this:Yes, BUT they mention the preventive therapy not the regeneration therapy
We are using silencing RNA technology to change supporting inner ear hair cells into sensory hair cells essential to hearing. Along with this, we are also working on restoring the connection between the auditory nerve and the hair cells that are disconnected when the hair cells die.
One of the aims of the research at HEI is to move the findings from the research bench to the clinic. Accordingly, the demonstration of the effectiveness of a combination of antioxidants on preventing hearing loss in animal models justified the funding of preclinical studies in humans and Phase I of FDA trials has now been completed. Our aim is to be able to obtain FDA approval within the next 3-5 years so that exposures to acoustic trauma both in civilian and military life need not lead to permanent hearing loss.
That's pharma for you. They will simply fail over and over again. Just sit back and laugh.I still don't get some companies whole antioxidant push. Why are they taking so much time to produce something that is a gloried multivitamin? Whats the payoff a margin improvement over multivitamins for a treatment that you have to apply within the first couple hours of noise damage. Its a kinda rhetorical question cause I know they will sell this to US military. But it just doesn't seem that ground breaking or useful imho.
really common and unfortunate among them
so I'm not sure it is clear that its a step forward.sure a step forward
Look at Antinitus, they had some approval that made their product believable.Yes, but there is also this:
They should probably formulate better what they mean by FDA approval, for what therapy, preventive or regenerative.
Stereocilias are part of these cell structures.Does anyone know if it's possible for stereocilia to be damaged by noise but the cell structures themselves [to] live on, despite this damage?
Tip links are extracellular tethers that link stereocilia, the tiny sensory projections on inner ear hair cells that convert sound into electrical signals, and play a key role in hearing.
https://medicalxpress.com/news/2013-06-two-step-mechanism-ear-link-regrowth.html
I would not wish or hope for that. Until we have a technology to peek inside a living cochlea and see what's actually damaged, it will all remain pretty much a guess work. Right now my own stereocilias, even if damaged, are probably doing a much better work than anything that scientists can come up with in a lab.I hope not, as I worry that the distortions I have in my hearing may be because of damaged rather than lost cells (that could potentially be replaced with a regenerative therapy)
I have heard different opinions on this. What you mean: is there sufficient cellular architecture post lesion for functional recovery of the organ. It is the 64 thousand dollar question. In severe acute neuritis of the vestibular organ, sometimes the disconnected canals begin to disintegrate a few months thereafter and the debris falls into the remaining functional canal causing secondary positional vertigo. Loose otoconia are also theorized to be a cause of menieres where the debris might clog up the various drainage systems of the ear. Whats interesting is that post postmortems often reveal different levels of remaining function. If the damage is localised to HC's themselves say for instance aminoglycoside poisoning you would theoretically still have fully functioning nerves under each, just with no sensory cell information to be passed down through the ganglion. But say it was a blunt trauma or a compression like a schwannomma this would essentially be an ischemic type injury that starves the ear cells of oxygenated blood, I have read in the literature before that a glass pipette placed over the primary vascular supply to the superior vestibular nerve (in mouse) for just 10 seconds can cause irreversible damage to the organ, so like the eye, the ear is "extremely" oxygen hungry. What we need is non invasive imaging of the ear that can show microscopic damage. What we need, is a time machine!Does anyone know if it's possible for stereocilia to be damaged by noise but the cell structures themselves live on, despite this damage? I hope not, as I worry that the distortions I have in my hearing may be because of damaged rather than lost cells (that could potentially be replaced with a regenerative therapy)
Stereocilias are part of these cell structures.
View attachment 12929
There are several different locations where you can have a damage. Stereocilias can break off at the root. They can also break without breaking off completely. There is also something called a tip link that links stereocilias together. These can break off as well.
View attachment 12930
I would not wish or hope for that. Until we have a technology to peek inside a living cochlea and see what's actually damaged, it will all remain pretty much a guess work. Right now my own stereocilias, even if damaged, are probably doing a much better work than anything that scientists can come up with in a lab.
What you describe as distortion may be the result of recruitment, yes.The distortions i guess are what we call recruitment right?
Very simply, recruitment is when we perceive sounds as getting too loud too fast.
recruitment is always a by-product of a sensorineural hearing loss. If you do not have a sensorineural hearing loss, you cannot have recruitment.
there are two other phenomena that often get confused with recruitment. These are hyperacusis (super-sensitivity to normal sounds) and phonophobia (fear of normal sounds resulting in super-sensitivity to them). Both hyperacusis and phonophobia can occur whether you have normal hearing or are hard of hearing. In fact, if you have a sensorineural hearing loss, you could suffer from all three conditions at once!
result of recruitment is "fuzzy" hearing. Since each critical band sends one signal at the frequency of that critical band, when hair cells get recruited into adjacent bands, they stimulate each critical band they are a member of to send their signals also.
The result is that we now often cannot distinguish similar sounding words from each other.
When this happens, basically all we hear is either silence or loud noise with little intelligence in it. Speech, when it is loud enough for us to even hear it, becomes just so much meaningless noise.
This is why many people with severe recruitment cannot successfully wear hearing aids. Their hearing aids make all sounds too loud—so that they hurt. Also, hearing aids cannot correct the results of our poor discrimination. We still "hear" meaningless gibberish.
http://hearinglosshelp.com/blog/recruitment-from-hearing-loss-explained/
I can only speak of my own experience. I had hyperacusis, and some phonophobia. After about 3 months it started getting better. This may depend on the severity of the damage. I have NIHL as a result of listening to music for long hours on headphones and earphones, and a recent acoustic trauma which is most likely the reason for my tinnitus.I have it also much less now after two months from my acoustic trauma but i hope its gonna get better
I understand recruitment is quite rare. You can find sound-bites on the internet to recognise recruitment. Provided you still have one "good" ear like I have.The distortions i guess are what we call recruitment right? I have it also much less now after two months from my acoustic trauma but i hope its gonna get better
I know this has been asked a billion times but, are we close? I don't want the "every day we draw closer" answer. I mean are we *really* close. Like, within 5 years?
Also, if a cure is found and someone who has tinnitus has it reduce drastically or even disappear all together could that person be exposed to loud noise again and have loud noticeable tinnitus again? Would they be able to use the cure again? How would that even work?
If tinnitus is and will be incurable, why are you wasting your precious time in a research forum?