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DaubersUP

12/01/18 10:57 AM

#250374 RE: DaubersUP #250373

I already sent this example to Leo. TIAB - you are doing your best to diminish the potential of the drug Brilacidin but your time is coming to an end here son. start packing up.

To infinity and beyond!

12/01/18 11:05 AM

#250375 RE: DaubersUP #250373

Leo never discloses bad news until forced to do so- haven't you noticed? BTD failure will be no different

PlentyParanoid

12/01/18 12:14 PM

#250382 RE: DaubersUP #250373

DaubersUP, your example manages to demonstrate two important things at the same time.

1. Significance of early BTD to companies working with substitute endpoints. In this case it is known that Hepatic venous pressure gradient (HVPG) does correlate with the stage of liver fibrosis. What is obviously not well known is what change in HVPG does constitute reliable indication of clinically meaningful change in NASH fibrosis. At least that seems to be FDA's view. Therefore, Galectin would have benefitted from applying for BTD as soon as possible i.e. before the start of p2 trial - they might have even managed to soften up FDA's requirements for meaningful change in HVPG with closer contact during the design of p2 trial.

2. Good example of what FDA requires for approval of BTD - reasonable clarity is good way of putting it.

TheDane

12/01/18 3:17 PM

#250389 RE: DaubersUP #250373

Naturally because the FDA hasn’t seen it before and they don’t understand it they reject it for BTD. That about right? How is any drug going to get BTD with that as the measure?

They put a fantastic spin on the rejection. I don’t think we’ll need it, however.

Go LEO!