Monday, March 27, 2017 3:38:25 PM
I'm just very curious, why is it taking so long to enroll the 30 Adjunct patients (even after the FDA reduction from 300 to 30 which was months ago)? I understand that the requirements for the screening are very strict, but you would assume there would still be at least a few dozen or so that would meet these? If the number of possible patients is so low, how will this data translate to the actual use of combination therapy of PRO-140 in the market where most of the people will not fall under these restrictions? Combination will still be a $1B/year market? If anyone can give a detailed answer, I'd very much appreciate it. Thanks in advance!
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