Frequency Therapeutics — Hearing Loss Regeneration

Would make sense to "fast track" it. It certainly is an unmet market.

What I´m hoping for is an "Open phase III", which mean we could get the drug as fast as 2 years from now.
That would be the fast "fast track" option.

Anybody know any examples where an "Open phase III" was being conducted?

I just heard about this as an option from someone on this forum.
The problem is "they" can always say hearing aids and cognitive therapies are part of the tinnitus market.

There are lobbyists in the FDA that are anti-treatment.
 
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A new video to pore over:


This is an excellent video to direct newcomers to this thread to. Thank you for posting!

The start date for new information regarding the efficacy of FX-322 has been confirmed to be the end of 2019. If the results of the study are positive, it would make sense for FX to release results ASAP in order to attract more funding.

Here's to hoping the end of 2019 will be a win for all! :beeranimation:
 
Where are the patients who were already treated with the drug? Why has not anyone come to tell us if they got good results? Is there a confidentiality agreement?
 
If it does not work, we can still expect scientists to invent the time machine :(
They have given the injections, now they are potentially periodically testing hearing with audiograms. If not, the subjects with the actual drug know.

They are also not locked up and if they have tinnitus and it's going away, then they are telling their friends, spouses, children etc.

The knowledge is out there somewhere.
 
They have given the injections, now they are potentially periodically testing hearing with audiograms. If not, the subjects with the actual drug know.

They are also not locked up and if they have tinnitus and it's going away, then they are telling their friends, spouses, children etc.

The knowledge is out there somewhere.
I think the company could give us some information about it, at least in a forum. It does not matter if they are in Phase I/II.
 
I think the company could give us some information about it, at least in a forum. It does not matter if they are in Phase I/II.
These things are strictly controlled by FDA regulations. This is a double blind placebo controlled study.

Official Title: "A Phase 1/2 Randomized, Double-blind, Placebo- controlled, Single-dose Study of FX-322"

https://en.wikipedia.org/wiki/Placebo-controlled_study


They cannot tell us anything, period, it will mess up the science. It makes sense. I just wish they would have tested the efficacy in this phase. Then there's the ugly consideration of proprietary and intellectual property, profits, and capitalism, that also induces another level of secrecy.
 
A new video to pore over:


Great speech. Regenerative medicine is the future. No other "treatments" come anywhere close.

Totally grasping at mere hints of infomation here but, 15:05 seems to imply that progenitor cells existed in patient, presumably at relevant frequencies, despite "severe" hearing loss (80 dB).
 
I don't know. It might give some direct awareness to their organization. Posting online is good too to gain awareness.
You have a point but don't worry, I'm sure they'll see the comment on their YouTube video too :)
 

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