RE: Patent & placebo nonsense3 Aug 2020 23:01
"Med3000 is a version of Dermasys that was reformulated specifically for the ED application!..."
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Dosanddonts, is almost correct. Yes, FUM reformulate the base Dermasys for each application, the aim is to maximise the transfer of the active ingredient through the skin barrier. That is correct. But it is the active ingredient that was 'specifically designed' for ED treatment and NOT the base dermasys (since renamed MED3000). It was very clever of someone at FUM (probably Ken) to suggest that it was MED3000 (base dermasys) that was 'specifically designed for ED'....very clever, very sneaky AND 100% unadulterated b0ll0cks!!!
The thing is, the base dermasys was 'designed' to be inert - hence all that GRAS references on their website. Base dermasys was renamed MED3000 and it was designed to be an inert carrier of the active compound. Hence why MED3000 was used as the 'placebo' in the P3 trial. It would have been a bit daft to have a randomized placebo-controlled trial when the placebo being used was actually 'specifically designed' to treat ED. As I say complete 100% b0ll0cks!!
FUM are leaving themselves open to an investor lawsuit for publishing misleading information IMO. And also creating an image - to potential pharma partners - as a company that isn't always truthful. The funny thing is that they don't need to try to fool us. Just stick to the truth FUM