Replies to post #8672 on Quanta Inc (fka QNTA)

[Fdc4]

Wrong!!! CEO already tried it in the DR buddy, on HUMANS AND it works!!! You are wrong on this. We are not years away, speed work nowadays!!!

[Rubberneck2]

If FDA gave approval for IND tomorrow, there would then be a 30 day wait until trials can commence. Multiple trial sites, recruitment of patients, 3 phases of trials unless the FDA allows a phase or two to be skipped based on evidence of safety and efficacy from studies outside the US. Minimum 1 year.

The way I see it FDA approval will be the icing on the cake. So much more to look forward to besides that.

[falon]

Not quite what FDA said.

QNTA already has done animal toxicology studies.

The FDA requested "TWO ADDITIONAL STUDIES".

FDA Accepts COVID-19 Clinical Study and Advises on Next Steps for Pre-IND Filing by Medolife Rx

As the Company expected, it received a detailed response from the FDA on its Pre-IND originally filed on April 27, 2020. The response included: recognition from the FDA on the therapeutic effects of Escozine®, validation of the Company’s clinical trial as an informal proof-of-concept study, and laid out very specific guidelines for the next steps required by the regulatory body in order to garner approval for Escozine® as a treatment for COVID-19.

Subsequent to the acknowledgement of the trial, the FDA has requested that the Company complete two additional toxicology studies in animals. Since adoption of COVID-19 vaccinations, the FDA altered its protocol for measuring toxicology to include studying it at the DNA level. As this is a newer development, the agency has asked Medolife to provide data in this regard. Medolife has the product and protocol necessary to complete these studies in short-order.

[Dapper10]

Quote: Basically the FDA said this drug isn't ready for any human trial yet. They're years away.

Truth: FDA DID NOT say this drug isn’t ready for human trial yet. The trial aren’t years away from testing. Non-Factual statement and 100% Bullshit.

[Dapper10]

QUOTE: Basically the FDA said this drug isn't ready for any human trial yet. They're years away.
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Totally non-sense and 100% Bullshit.
They are already testing humans in the DR and no problems noted. The US FDA will wake up very soon and realize Escozine is the real deal and approve. When they realize the current Vaccine being given really isn’t a true vaccine but only a Gene Therapy. A true Vaccine is what we all got to stop Polio. What everyone is taking is an experimental drug only and a % of people are dying from these drugs. Nobody has died from taking Escozine and that’s why the FDA must approve Escozine to start saving lives and not killing them. My opinion.