Isn't that basically the same as them using a placebo? If just care has the same effect, then surely heavily monitoring them while providing a placebo drug should work.
The problem is you can very obviously tell that you have a placebo because nothing is happening. Some studies mitigate that issue by giving a microdose but then maybe only the microsose is necessary? It seems like a hard problem
"In this phase 2b, multicenter, randomized, double-blind, placebo-controlled study of 4 dose levels of MM120 that included 198 adults with generalized anxiety disorder, the primary outcome of a dose-response relationship for change in Hamilton Anxiety Rating Scale score at week 4 was statistically significant."
Unfortunately, I will probably never be able to try that for my GAD even if they confirm the positive effects due to stigma surrounding psychoactive drugs! Yay!
mhm where i live you can go to a hydro grow store and buy the spores that you definitely SHOULD NOT inject into the aio grow bag conveniently placed nearby lol
I’d be afraid of a treatment like this where you’re sort of different after one treatment. From experience taking ssris, I took one one that worked so well that I had to stop taking it because it removed stress to the extent that I wouldn’t get to class on time or get my homework done before deadlines. Eventually I found a medicine that worked for me. But, if there’s a “before” vs “after” one shot treatment, you have to hope the new you is the one you want assuming you could be stuck there permanently.
When you have heavy generalized anxiety, you are usually willing to commit to that if it means there is a significant probability of coming out with an improved condition. I had such terrible panic attacks before my treatment with a bunch of different medication that I seriously considered and searched for electroconvulsive therapy and even help from shady religious institutions.
I might have gotten that desperate myself, but I finally found a great physiatrist that gave a shit and was competent. Simply taking Effexor removed my panic attacks without problematic side effects.
Yeah, changing psychiatrists also helped me. Unfortunately, I had to change drugs a couple of times and ended up taking multiple ones to end my panic attacks. Those drugs left me with long lasting tremors, even after I've stopped taking them, but the tremors are 10000x better than the panic attacks.
I think curing GAD will mean changing your personality. There's always going to be a before/after you, that's the whole point. The important part is being able to reliably know what the "after you" will be so you can be sure that you want that change to happen.
Curing anything changes your personality. I stopped biting my nails to the quick after 50 years - that's a difference!
The Ship of Theseus argument should never be used to justify retaining mental dysfunction. "What if I can't paint sunflowers if I stop being suicidal?" is a question; more decades of Van Gogh paintings would inarguably have been better.
A good point, but if stress was your motivator, it might be better to work to reframe that and gain motivation through something else that isn't stress.
HN has some peculiar medical fixations. It comes in waves. For a while there were a lot of submissions about intermittent fasting. 15 years ago people were excited about polyphasic sleep. 10 years ago it was all about modafinil. Enthusiasm about ketamine for depression was big, but it seems to have finally fizzled out.
To an extent I feel your position, and it can be true in many contexts. I would say, however, that taking a trip to a far off country, and dropping acid serve two different purposes. While I'm sure there's some overlap, you won't get the entirety of the experience from either one exclusively.
"Today a young man on acid realized that all matter is merely energy condensed to a slow vibration, that we are all one consciousness experiencing itself subjectively, there is no such thing as death, life is only a dream, and we are the imagination of ourselves. Here's Tom with the weather."
today an evolved monkey realized that the evolution of intelligence via genetic algorithms doesnt line up that well with the scientific trajectory of existence since the big bang , he then realized that his perception of existence would be exactly equivalent to that of a brain in a jar , his final realization was that all realizations are epheremal regardless as to how convincing or conclusive they may seem
This reflects a longstanding...essentially conspiracy...to suppress attention to 5HT2A-based neural regulation because it sheds such poor light on SSRIs
But if you catch me in a get-together setting and we share a beer together, I'd say: "on the one hand you have a well-determined profitable path in the SSRIs, and on the other hand you have people giving LSD doses away for free to each other. One sits well, one doesn't. One has to wonder why the people aren't giving away SSRIs for free if they work so well, right?"
The "neuroplasticity" which leads to a relative quietness presumably comes after the psychedelic experience.
Interestingly, the paper only lists the following adverse effects: visual perceptual changes, nausea, and headache. Given that the patients in the double-blind study were those who suffer from moderate to severe Generalized Anxiety Disorder, I could imagine some significant anxiety in the 200 µg active group!
The paper only reports significant results at the 100 µg and 200 µg dose level, not less, which seems like another strike against psychedelic microdosing. The pharmaceutical industry would love to find a magic psychedelic drug which doesn't result in the psychedelic experience, but it seems like that experience is the key to their mental impact.
Of course they want to repackage a cheaply synthesized substance at 100-1000x the costs even though the original likely works just as well. That's pharma for you.
The "surprising way" is by using a derivate of LSD.
I'd argue that the surprise is rather on this: "In clinical trials, a single dose significantly outperformed standard treatments, offering hope to those who have found little relief elsewhere."
It is no derivate. It's just the tartrate salt of LSD. There is no pharmacological difference. It's like saying I got this new Magnesium Tartrate which is now different to the Magnesium Oxide / Citrate / Glycinate / whatever you are taking. It might affect stability or absorption rate or similar, but Tartrate itself doesn't have an effect.
I agree. I have anxiety sometimes, but I’m not about to start taking LSD. I’m not going to risk a permanent psychological crisis to reduce my anxiety. It’s not really a cure if it has a even a small percentage chance of causing something much worse.
Calling it the "pharmaceutical form" is borderline misinformation, considering it's just a common salt of LSD. You can get that outside the pharmacy. It's not like actual LSD is ever made in some dirty improv meth lab. Likewise, nobody expects researchers to buy their drugs on the streets. It's just LSD. This "say no to drugs" drug did the trick.
No. That is a gross and deliberate mischaracterization in bad faith. Here is the full quote:
> Side effects were generally mild or moderate and included hallucinations, visual distortions, nausea, and headache. It's important to note, these were more prevalent using the highest dosage -- which we will not be using since it was found to be no more effective.
I'd argue that the results might not be from the drugs but from the fact that they were heavily monitored by other humans.
It's not the drugs that people with high anxiety need, it's people giving them attention and caring for them.
These experiments need a control where they just take the drug and they don't have medical staff around.
Isn't that basically the same as them using a placebo? If just care has the same effect, then surely heavily monitoring them while providing a placebo drug should work.
But that doesn't test if the LSD helps in a non-clinical setting, only that the monitoring and attention helps
The problem is you can very obviously tell that you have a placebo because nothing is happening. Some studies mitigate that issue by giving a microdose but then maybe only the microsose is necessary? It seems like a hard problem
"In this phase 2b, multicenter, randomized, double-blind, placebo-controlled study of 4 dose levels of MM120 that included 198 adults with generalized anxiety disorder, the primary outcome of a dose-response relationship for change in Hamilton Anxiety Rating Scale score at week 4 was statistically significant."
The control is where you have the medical staff around but not the drug. I believe placebo control groups are pretty common.
You are fabricating a lot of details about the study to come to that conclusion.
If only there were experts on the ground, designing the experiment, who could plan to avoid such interfering variables.
Unfortunately, I will probably never be able to try that for my GAD even if they confirm the positive effects due to stigma surrounding psychoactive drugs! Yay!
Why? Stigma from whom?
MM120 is seeking FDA approval and there are many more in late stage trials for GAD.
Nitpick: you will probably never be able to try it legally.
There are lots of ways you could try LSD tho.
psilocybin is easy to find (even legally, in certain jurisdictions) or cultivate yourself.
LSD and psilocybin are very different. Wouldn't think it, but it's true
mhm where i live you can go to a hydro grow store and buy the spores that you definitely SHOULD NOT inject into the aio grow bag conveniently placed nearby lol
Some will sell an already conolized growbox. Much harder to fail than the spores.
I’d be afraid of a treatment like this where you’re sort of different after one treatment. From experience taking ssris, I took one one that worked so well that I had to stop taking it because it removed stress to the extent that I wouldn’t get to class on time or get my homework done before deadlines. Eventually I found a medicine that worked for me. But, if there’s a “before” vs “after” one shot treatment, you have to hope the new you is the one you want assuming you could be stuck there permanently.
When you have heavy generalized anxiety, you are usually willing to commit to that if it means there is a significant probability of coming out with an improved condition. I had such terrible panic attacks before my treatment with a bunch of different medication that I seriously considered and searched for electroconvulsive therapy and even help from shady religious institutions.
I might have gotten that desperate myself, but I finally found a great physiatrist that gave a shit and was competent. Simply taking Effexor removed my panic attacks without problematic side effects.
Yeah, changing psychiatrists also helped me. Unfortunately, I had to change drugs a couple of times and ended up taking multiple ones to end my panic attacks. Those drugs left me with long lasting tremors, even after I've stopped taking them, but the tremors are 10000x better than the panic attacks.
I think curing GAD will mean changing your personality. There's always going to be a before/after you, that's the whole point. The important part is being able to reliably know what the "after you" will be so you can be sure that you want that change to happen.
Curing anything changes your personality. I stopped biting my nails to the quick after 50 years - that's a difference!
The Ship of Theseus argument should never be used to justify retaining mental dysfunction. "What if I can't paint sunflowers if I stop being suicidal?" is a question; more decades of Van Gogh paintings would inarguably have been better.
A good point, but if stress was your motivator, it might be better to work to reframe that and gain motivation through something else that isn't stress.
It seems like every few weeks there's an article on how drugs are amazing hitting the front-page.
HN has some peculiar medical fixations. It comes in waves. For a while there were a lot of submissions about intermittent fasting. 15 years ago people were excited about polyphasic sleep. 10 years ago it was all about modafinil. Enthusiasm about ketamine for depression was big, but it seems to have finally fizzled out.
Ketamine is still used for depression quite effectively.
It's good that techbros' interest in it fizzled out though. Better for everyone that way.
Wonder what the approach would be to empirically determine these waves.
Where do you go when you need to escape but can't actually go anywhere?
Inwards. Imagination, media, substances, meditation, solitude.
To an extent I feel your position, and it can be true in many contexts. I would say, however, that taking a trip to a far off country, and dropping acid serve two different purposes. While I'm sure there's some overlap, you won't get the entirety of the experience from either one exclusively.
Well... drugs are amazing. They're so amazing people will literally die for them.
At the risk of sounding like an imbecile, can I ask why LSD-25 can't be the pharmaceutical form of LSD?
"Today a young man on acid realized that all matter is merely energy condensed to a slow vibration, that we are all one consciousness experiencing itself subjectively, there is no such thing as death, life is only a dream, and we are the imagination of ourselves. Here's Tom with the weather."
-Bill Hicks
today an evolved monkey realized that the evolution of intelligence via genetic algorithms doesnt line up that well with the scientific trajectory of existence since the big bang , he then realized that his perception of existence would be exactly equivalent to that of a brain in a jar , his final realization was that all realizations are epheremal regardless as to how convincing or conclusive they may seem
Hell yeah man. Momentary lapse.
Thanks for reminding me of this. One of the all time greats.
Tool.
In case others don't know, Tool used this quote in their song Third Eye.
It's more than just a quote, it's a sample of Bill Hicks himself speaking it.
This reflects a longstanding...essentially conspiracy...to suppress attention to 5HT2A-based neural regulation because it sheds such poor light on SSRIs
I land on "if it helps it helps."
But if you catch me in a get-together setting and we share a beer together, I'd say: "on the one hand you have a well-determined profitable path in the SSRIs, and on the other hand you have people giving LSD doses away for free to each other. One sits well, one doesn't. One has to wonder why the people aren't giving away SSRIs for free if they work so well, right?"
It is tragically funny to consider linking quietness of mind with LSD. It is everything but quiet
The "neuroplasticity" which leads to a relative quietness presumably comes after the psychedelic experience.
Interestingly, the paper only lists the following adverse effects: visual perceptual changes, nausea, and headache. Given that the patients in the double-blind study were those who suffer from moderate to severe Generalized Anxiety Disorder, I could imagine some significant anxiety in the 200 µg active group!
The paper only reports significant results at the 100 µg and 200 µg dose level, not less, which seems like another strike against psychedelic microdosing. The pharmaceutical industry would love to find a magic psychedelic drug which doesn't result in the psychedelic experience, but it seems like that experience is the key to their mental impact.
You're describing what's called a critical period.
These are well established and lots of research is going on as to why psychedelics seem to put us into a critical period.
Lsd, psylocybin and mdma all seem to do it. Peyote does too.
While in the critical period, usually a week to 3 months, it is very important to surround oneself with what they want to focus on.
Of course they want to repackage a cheaply synthesized substance at 100-1000x the costs even though the original likely works just as well. That's pharma for you.
The "surprising way" is by using a derivate of LSD.
I'd argue that the surprise is rather on this: "In clinical trials, a single dose significantly outperformed standard treatments, offering hope to those who have found little relief elsewhere."
It is no derivate. It's just the tartrate salt of LSD. There is no pharmacological difference. It's like saying I got this new Magnesium Tartrate which is now different to the Magnesium Oxide / Citrate / Glycinate / whatever you are taking. It might affect stability or absorption rate or similar, but Tartrate itself doesn't have an effect.
Why can't they just put it in the title of the article instead of classic clickbait tactics? Ugh.
I agree. I have anxiety sometimes, but I’m not about to start taking LSD. I’m not going to risk a permanent psychological crisis to reduce my anxiety. It’s not really a cure if it has a even a small percentage chance of causing something much worse.
> The "surprising way" is by using a derivate of LSD.
What's the difference between a derivate and a derivative?
(I'm not being facetious, I'd really rather like to know)
Calling it the "pharmaceutical form" is borderline misinformation, considering it's just a common salt of LSD. You can get that outside the pharmacy. It's not like actual LSD is ever made in some dirty improv meth lab. Likewise, nobody expects researchers to buy their drugs on the streets. It's just LSD. This "say no to drugs" drug did the trick.
Clickbait
"Side effects were mild or moderatr and included hallucinations..."
Yeah....
No. That is a gross and deliberate mischaracterization in bad faith. Here is the full quote:
> Side effects were generally mild or moderate and included hallucinations, visual distortions, nausea, and headache. It's important to note, these were more prevalent using the highest dosage -- which we will not be using since it was found to be no more effective.