Please help, to our scientist and those with knowledge of the FDA

With all the great news about ABL, it would appear ABL becomes a blockbuster!

What does it take at this point to get FDA approved study?  Does RVX have the staff to prepare the report to request a P1 study or a P2 study reducing the effects COVID19?  What time frame, documentation, and funds necessary to apply for study?  Not the P1 or P2 funding, just the application?

Wondering if RVX has the ability or do they need to go outside, what would a third party charge and is there sufficient data available?

If RVX has the internal ability to develop and submit a plan, it may be easier to find a partner. 

Many questions here, have not read this in our forum.  

Thank you, stay safe, it is not over, sidebar.