That's the absolute limit I believe.My DPOAE went up to 10 kHz.
That's the absolute limit I believe.My DPOAE went up to 10 kHz.
Regarding trial design, I'm really curious if anyone has any good rebuttals to my bear thesis on the game theory from the perspective of the "cheater." I think I make pretty good arguments as to (a) why the cheating wouldn't help the placebo group more and (b) in the cases where it does, it's a bad reflection of the drug.
Hey, I just came by after the Phase 2a results to say I told you so, but I really had no idea.If an effective treatment for tinnitus ever emerges, the entire world will know about it in very short order. It will be all over the 10 o'clock news.
The medical profession will be full of it.
In the meantime I'll avoid all the furore, and the unnecessary excitement - I do so hate wetting my pants - and carry on just as before.
I'll get excited when there is some evidence based proof of successful results.
I'm a pragmatist.
Jazzer
Buying biotech stock is supporting research. Without the investors on board taking the huge risks, research wouldn't advance and clinical trials wouldn't happen. Biotechs have a high failure rate.If you ask people to financially support Tinnitus Talk, or research, they don't have the money.
But they have enough money to buy stock...
I'm curious why you post in this thread then. You've now said twice in 24 hours how this doesn't interest you, everyone knows it now. Others here, in the meanwhile, want to stay informed about research. To each his own.Listening to interviews with medical researchers, scientists, doctors, etc... does nothing for me.
Hearing about the 'nitty-gritty' of their research programme does nothing to ease the experience of tinnitus.
Yes - of course I am pleased that research goes on because we clearly need a treatment, but as yet there is no prize to report on, or get excited about.
I don't need a detailed report on what the mechanic intends to do to try to fix my car.
Just let me know when the bloody thing is going again.
Good answer ajc.I'm curious why you post in this thread then. You've now said twice in 24 hours how this doesn't interest you, everyone knows it now. Others here, in the meanwhile, want to stay informed about research. To each his own.
Yes, both ongoing studies got them as Secondary Outcome Measure. Point No. 4.Question: do any of the ongoing single-dose trials have EHF audiograms as an experimental outcome? I'd like to see that given another shot (no pun intended) without the apparently detrimental multi-dosing effect.
OK, good to know that (and TFI) will continue to be looked at in ongoing and presumably forthcoming trials. The Phase 2a report was so discouraging that I feel like it can only get a little better from here. I wish all of us some comfort and maybe some reasonably modest life improvements in the meantime, as we wait for science to do its glacially-paced work.Yes, both ongoing studies got them as Secondary Outcome Measure. Point No. 4.
Adults With Severe SHL:
https://www.clinicaltrials.gov/ct2/show/NCT04629664
Adults With Age-Related SHL:
https://www.clinicaltrials.gov/ct2/show/NCT04601909
Because they already saw improvements in WR and Audimetry by day 90 from previous Phase 1/2 study.Why do the two Phase 1 trials go until day 90 and not day 210? The last report will be on day 90?
Hearing / tinnitus may take time to improve; we don't know, some testimonies point in this direction.
Because they are primarily safety studies in new treatment populations with some measures that could be used to evaluate safety and efficacy.Why do the two Phase 1 trials go until day 90 and not day 210? The last report will be on day 90?
Hearing / tinnitus may take time to improve; we don't know, some testimonies point in this direction.
Or hopefully at least hear of such delayed improvements via the same informal communication (through the ENTs) that informed them of earlier tinnitus anecdotes, so they might consider doing later follow-ups in future trials.So if tinnitus takes time, that wouldn't be known before that point unless they go back later and interview Phase 1b participants.
I agree for severe / age-related hearing loss Phase 1b phases, even if the safety has already been proven.Because they are primarily safety studies in new treatment populations with some measures that could be used to evaluate safety and efficacy.
Phase 2a was the efficacy trial. A redo of Phase 2 would be a longer monitoring period with different trial design and dosing. So if tinnitus takes time, that wouldn't be known before that point unless they go back later and interview Phase 1b participants.
Maybe they will report it as "long term follow up" separate from the trial like they did with the Phase 1 results.I agree for severe / age-related hearing loss Phase 1b phases, even if the safety has already been proven.
But is there a phase with a single injection (where there was 10% improvement in 32% of people)? We will not have day 210 results for this trial?
Firstly, buying biotech stock is support only if you take part in IPO or during capital raise. If you buy FREQ after that, it is not support at all.Buying biotech stock is supporting research. Without the investors on board taking the huge risks, research wouldn't advance and clinical trials wouldn't happen. Biotechs have a high failure rate.
I do both. So do many members here who hold stock and contribute to this community. The members here who invest their time supporting others and discussing research are investing their time here.
The people on stock boards looking to just to make cash probably have little interest, apart from financial motivation, for it to succeed. That's what makes the world go round after all.
Even though I lost most of my investment and pulled out as I have lost confidence in FREQ, I still contribute to Tinnitus Talk and will continue to do so as I can afford it.
Everybody who uses Tinnitus Talk especially for the discussion of research should be contributing if they can afford to do so. It also beats sending money to a charity that I have no idea what they do with it; or who in the past have been promoting shit like TRT.
Err... not exactly. And you should know this if you're commenting on it.Firstly, buying biotech stock is support only if you take part in IPO or during capital raise. If you buy FREQ after that, it is not support at all.
Frequency Therapeutics Releases New Data from Two FX-322 Clinical Studies; Plans to Advance Single-Dose RegimenI agree for severe / age-related hearing loss Phase 1b phases, even if the safety has already been proven.
But is there a phase with a single injection (where there was 10% improvement in 32% of people)? We will not have day 210 results for this trial?
So the incidence rate of 10% or more improvement rose with multiple doses?...
So far, these are their official announcements.
It's nice to have this all in one place. I didn't realize they released this.
Different study. They found the inconsistencies in Phase 2a.I suppose the subjects that more than doubled their WR score will be the same who faked their WR score in recruitment the most.
No, those are legit, FDA and peer reviewed.I suppose the subjects that more than doubled their WR score will be the same who faked their WR score in recruitment the most.
Are you sure that all their studies were non-faked? Do they even know that there is something like ASSR test?Different study. They found the inconsistencies in Phase 2a.
I must say, I find it surprising that they say this (attached) so boldly.It's nice to have this all in one place. I didn't realize they released this.
I get what you are saying but there is something very unique about this trial that I feel not enough weight is put on it.I must say, I find it surprising that they say this (attached) so boldly.
View attachment 44498
That's an awful lot of confidence without individual data.
I'm starting to get kind of irritated at the notion that this problem is unique to Frequency Therapeutics. Literally every placebo-controlled medical study has the same basis:
Why doesn't every trial that failed just say this? To be clear, I'm not mad that they are pointing this out. I'm mad that they can do this without individual data as an out for a drug that was otherwise underwhelming.
- A problem is being treated that is inherently challenging to have objective measures for
- Person wants to get into the study in order to have a chance at early treatment
- The participants have a bias to be the best to show off the drug
I get what you're saying about genuine challenges in obtaining this specific patient class.I get what you are saying but there is something very unique about this trial that I feel not enough weight is put on it.
A person with low word scores but who has below severe audiogram changes is a very unusual patient.
They are selecting from a low pool of genuine patients.
And in doing so, selection pressure *greatly* favors the word score depressors in Phase 2a, where it was a requirement.
This greatly affects the degree in which this kind of skews results.
I should add @Zugzug that social media plays a role and there likely have been way more "trial design failures" in recent years based on this but, in particular, when an extremely narrow patient is recruited.