"In phase 1 clinical trials, the safety, tolerability and toxicity of the drug at different doses is tested in a small number of healthy volunteers. In phase 2, the drug's efficacy and optimal dosing regimen are established.
After phase 2, the drug enters the most vital stage of its development, the phase 3 trial. This is the last phase of testing the drug needs to complete before the drug information and clinical trial results are submitted to the regulatory authorities for approval of the drug for use in the general population.
The phase 4 trial is also referred to as post marketing surveillance and as the name suggests, it is conducted after the drug is already marketed and available to the general public. The main objective of the phase 4 trial is to check the drug's performance in real life scenarios, to study the long-term risks and benefits of using the drug and to discover any rare side effects.
In a phase 4 trial, any rare or long-term effects of the drug can be observed in a much larger population of patients and over a much longer period of time. If safety surveillance does indeed reveal concerns about the drug, it may be withdrawn from the market and no longer made available on prescription."
My first reaction was one that would get me arrested. (Watergate stuff, not any more violent coercion - that would still be a far lessor crime than the murder and maiming of defenceless innocents!)
Not every country has a "stone-walling", "the process is the punishment" legal system.
If people like Judicial Watch in the US can get lots of sensitive material released under FOIA's in the US, then European, Australasian, East European, South and Latin American countries and African countries can do the same.
But, I hear what lies behind your question. "Proprietaty".
Apologies, I thought the Phase III trials are ongoing via the general population, and will end formally in March of 2023?
Phase 3 is designed to prove safety and efficacy in a large sample population (injected b placebo). Phase 4
https://www.news-medical.net/health/What-is-a-Phase-4-Clinical-Trial.aspx
"In phase 1 clinical trials, the safety, tolerability and toxicity of the drug at different doses is tested in a small number of healthy volunteers. In phase 2, the drug's efficacy and optimal dosing regimen are established.
After phase 2, the drug enters the most vital stage of its development, the phase 3 trial. This is the last phase of testing the drug needs to complete before the drug information and clinical trial results are submitted to the regulatory authorities for approval of the drug for use in the general population.
The phase 4 trial is also referred to as post marketing surveillance and as the name suggests, it is conducted after the drug is already marketed and available to the general public. The main objective of the phase 4 trial is to check the drug's performance in real life scenarios, to study the long-term risks and benefits of using the drug and to discover any rare side effects.
In a phase 4 trial, any rare or long-term effects of the drug can be observed in a much larger population of patients and over a much longer period of time. If safety surveillance does indeed reveal concerns about the drug, it may be withdrawn from the market and no longer made available on prescription."
The rise of variants is working now ;) thanks again.
sorry, thought you meant the latypova one.
That’s ok. My bad I just thought they removed the video already.I have watched some of Mrs. Latypova videos. 👍🙏
How do we demand this from our governments?
My first reaction was one that would get me arrested. (Watergate stuff, not any more violent coercion - that would still be a far lessor crime than the murder and maiming of defenceless innocents!)
Not every country has a "stone-walling", "the process is the punishment" legal system.
If people like Judicial Watch in the US can get lots of sensitive material released under FOIA's in the US, then European, Australasian, East European, South and Latin American countries and African countries can do the same.
But, I hear what lies behind your question. "Proprietaty".
Do you have another link for the video ? For some reason won’t open or play
deleted
try this
https://childrenshealthdefense.org/video-post/moderna-clinical-trials-terribly-flawed-and-fda-knew-it-sasha-latypova-tells-rfk-jr-2/
or this]
https://podcasts.apple.com/us/podcast/leaked-moderna-files-with-sasha-latypova/id1552000243?i=1000574962396
Thanks