Please explain which vaccine you think is a gene therapy and why you think that it is a gene therapy.
If you asked anyone at Moderna in 2018 what they were experimenting with that would have said it was a gene therapy that makes your body produce vaccine. Suddenly in 2020 they reclassified it as a vaccine, to make it sound like traditional and well proven technoloigy.
Do you have any source to support that claim? (Both that they earlier called mRNA vaccines gene therapies, and that the reason why they changed that was "to make it sound like traditional and well proven technoloigy")
Also, why do you think that the former classification was more accurate than the current one?
Also, why are you giving a cut-off date of 2018, given that the vaccines for a disease that appeared in 2019 obviously was tested after 2018? Like, is there a specific reason why you are excluding the test of the vaccines in question themselves when trying to support your claim that things didn't work well?
The latest things I've seen about experiments with mRNA vaccines prior to the COVID one are from 2017 and 2018.
You did notice that that doesn't answer my question?
Is there any medical treatment that you would not consider experimentation on people?
Real vaccines, of a type with a long safety track record, launched after full scale trials, and used with a proper authorisation, rather than an emergency one, aren't experiments. They still need to be used with care, though. We dodged a bullet with a fairly conventional swine flu vaccine that turned out to have horrible consequences not picked up during trials. Luckily it was not widely used.
I am not sure I understand what your argument is.
As you yourself write, other vaccine technologies with a long track record at times go horribly wrong. Why would that be a reason to prefer those?
That especially so given that you yourself also name as the primary problem with mRNA vaccine research in the past was lacking effectiveness, not lack of safety, so it's not like mRNA vaccines had no safety track record--even if you discard a vaccine because it isn't effective, the trial still builds safety track record, after all.
Also, it is unclear to me what you consider "full scale trials" or "proper authorisation", or why you think that "emergency authorisation" makes somehow a binary difference between "experimentation" and "not experimentation".
I mean, no vaccine is guaranteed to be 100% safe, you yourself giving a prominent example. No amount of clinical trials can change that. Now, of course, in some sense, every vaccination, just like every other medical treatment, is an experiment of sorts, in that you never know whether in that one patient you will suddenly see some side effect that was never seen before, or that was never tied to the treatment as the cause, and that every application of the treatment thus contributes to figuring out just how safe a treatment is, and under which conditions it is dangerous. So the difference between "experimental" treatments and "tested and approved" treatments is unavoidably somewhat arbitrary, in that the experts who do that kind of work analyze statistically what the remaining risks are, and then declare things "tested and approved" once the calculated risk is lower than some selected threshold.
Now, as far as I can tell, the only difference between a "normal authorization" and an "emergency authorization" is how high you set that threshold. I.e., when there is an ongoing pandemic where people are dying in large numbers, plus all the other bad effects from infections, a higher risk for a treatment is considered acceptable, because waiting for a lower threshold to be reached itself has a risk for people.
But that also is nothing fundamentally special about emergency authorizations. If you try to get a new treatment authorized that shortens the common cold by a day (i.e., where the risks from the illness itself are essentially non-existent), you'll have to meet a much stricter risk standard than if you try to get a treatment authorized that cures some highly aggressive cancer. If the former kills one of a thousand users, that would be completely inacceptable. If the latter kills one in ten, that might be perfectly acceptable.
Of course, you couldn't know for absolutely certain whether any of the vaccines would turn out to have some bad long-term effects. But you couldn't know the same about the illness itself, which obviously was to be expected to infect everyone rather sooner than later. And looking back, long covid seems to be a much larger problem than damages from vaccination. That is why emergency authorizations are a thing.
Also, I just want to point out what you are shifting goal posts. Before, you were claiming that people's human rights were violated with vaccination mandates. Now, you are only talking about one specific vaccine technology, even though vaccines based on other technologies were available, so noone was required to use these specific vaccines.
How many people were able to choose which vaccine type they got? In the UK we had the Astra Zeneca vaccine, which was another new technology, but that seemed to have problems, and was withdrawn. After that we only had the Moderna and Pfizer mRNA vaccines available here. As far as I know problems with the J&J vaccine in the US lead to only the mRNA ones being available there, too.
Over here, people could get either of those vaccines if they really wanted. Like, not every vaccine was necessarily available everywhere at any time, but you should have been able to find the one you wanted if you had a preference.
Of course, as more data came in and the virus mutated, availability of vaccines changed, but IIRC, when vaccination mandates were relevant, you still had the choice.
There wasn't just one problem with the way governments ignored decades of pandemic planning, and went rogue. There were quite a few.
Well, that might be true or not ... but isn't really relevant here, is it?