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AGORACOM NEWS FLASH

Dear Agoracom Family,

I want to thank all of you for your patience with us over the past 48 hours and apologize for what was admittedly a botched launch of our new site.

As you can see, we have reverted back to the previous version of the site while we address multiple forum functionality flaws that inexplicably made their way into the launch.

To this end:

1.We have identified 8 fundamental but easily fixable flaws that will be corrected in the coming week, so that you can continue to use the forums exactly as you've been accustomed to.

2.Additionally we will also be implementing a couple of design improvements to "tighten up" the look and feel of the forums.

Have a great Sunday, especially those of you like me that are celebrating Orthodox Easter ... As well as those of you who are also like me and mourning another Maple Leafs Game 7 exit ... Ugggh!

Sincerely,

George et al

Message: Re: 3rd Quarter Financial Statements

BDAZ – Last I heard was the DSMB’s next report would be out around mid March, that’s today. If they are off by a week or so I wont lose any sleep and no one else should either. I am not aware of any pre-defind DSMB review dates.

You asked “what did you mean by “hopefully not hearing from the FDA on the Kidney trial application before the 25th of March”

I have heard from RVX in prior meetings as well as from at least 3 other biotech companies that once their IND is filed or the completion of this Type B meeting with the FDA has happened that the FDA has 30 days to respond to them if there is a problem that needs to be addressed. If there is no response within those 30 days then the results of the meeting or IND application are acceptable the way they are. The 25th of March represents the 30th day after 23 Feb. Worth noting is that the 25th of March is a Saturday so any response would have to be prior to the 25th as I stated.

In my opinion this would be incredibly good news as we would have one division of the FDA accepting RVX208 and then just have to wait for the other division to do the same. Essentially this could be the start of doubling our potential market from where it is today. This is worth getting excited about.

Further information about the steps involved in getting FDA approval can be found at  https://www.fda.gov/ForPatients/Approvals/Drugs/ucm405622.htm

 

 

tada

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