Member Info for Bucolic

Jonah, are you ok? It sounds like you're regressing even more.

Like you, Baggo, I think cbd is too much of a niche market to generate much profit for investors. FUM says they have an innovative and unique product, but they always say stuff like that. Bad luck on Celebrity Masterchef, by the way.

Perhaps baldy prefers another song of theirs - "I'm undecided".

Crusader, just because FUM's website uses the term doesn't mean it's the correct term. They have a certain way with words that slants the meaning in their favour, for instance claiming that MED3000 went through clinical trials. Of course, it did, but not as the subject of the trial. Claiming that their ingredients to be GRAS is just a bit more smoke and mirrors. I'm not disputing that the ingredients are safe, just that GRAS is a term used by US Congress to define food additives. It's all there on the FDA website. It may even be true that the GRAS classification has been applied, but it has no relevance to a medical device.

The.Italian says GLA. Presumably that's "GOOD LUCK ARSENAL!"

Oh, forgot to mention the pizza and Chianti afterwards. I'm living my best life! I see you've given Baldy another word to mull over - crotchety!

You took the words right out of my mouth, The.Italian. I managed to retire at 59. how about you? I must say I'm looking forward to this afternoon's game. The Mighty Arsenal, a few homebrewed American IPAs, bliss!

There are none so deaf as those who will not hear. So lets talk about why you decided that the FDA didn't say there was to be a trial, instead of making assumptions about me. (illogical ones at that.) After all, no one is interested in me, just FUM, which is why they are here.

Sorry, I meant Jonah, not Frank. Oh well, soon be beer o'clock!

Frank, I don't do wages anymore. My money comes purely from the stock market, which is why I felt the need to call you out for trying to spread an untrue story. I know you and many others assume I'm deramping, but why would I do that when I'm invested in FUM? I'm just very annoyed at the way they're going about things and costing me money. I apologise if you thought I was being nasty, but everyone knows about the new trial ffs!

I've got an image in my mind of Frank, Jonah and sb88, sitting in a circle in the nursery, fingers in their ears, eyes squeezed shut, chanting "nanananananana Ican't hear you nananana!"

Jonah, DYOR. It's common knowledge about the extra trial. I know you're sitting on a beach so I think the sun must have gone to your head. Did you not spot the drop in SP after the last RNS? Here, don't bother getting off your ass, here's a bit from the rns of the 14th. - "The FDA have indicated a requirement for certain additional clinical efficacy data beyond the Company's three months' home use study conducted in 2019 in 1,000 patients suffering from mild, moderate and severe ED ("FM57"). This additional data will require a further small clinical trial where patients with ED will receive MED3000 for a six month treatment period. "

Hold on a minute! Have I missed something? Have the FDA about-turned and said MED3000 DOESN'T need another trial?!! Or are sb88 and JONAH talking out their backsides again? (Rhetorical question, obvs.)

I see our tame professor, David Ralph, is in the news today. A bit off-topic here, but there's a story in the Daily Mail today about a mechanic from Norfolk whose knob rotted away and fell off. Professor Ralph only made him a new one - on his arm! It's been due to be transferred to his knacker area since 2018 but has been put off several times for various reason, leaving matey to wander around with his member on his left forearm! Let's hope he doesn't splash his hand gel around too much, eh Odysseus!

crusader, as a medical device I doubt if the FDA will take into account whether MED3000 is GRAS or not. Even if they did, it would only require a notification to the FDA, rather than a trial. The FDA website says this: "Congress further stated that 'substances that are generally recognized, among experts qualified by scientific training and experience to evaluate their safety as having been adequately shown . . . to be safe under the conditions of their intended use,' are excluded from the definition. Put simply, substances that are GRAS under conditions of their intended use are not food additives and do not require premarket approval by FDA."

Well, you've certainly cemented your deramping credentials there, Ody.

Given your last post, Ody, I take it you won't be investing. BTW, the evaporation and cooling explanation is merely guesswork, as they don't really know why it works, but you keep mentioning it as fact. And your suggestion for people trying out their hand gel tonight is only applicable if people have ED issues, otherwise it's pointless.

I'm not forgetting anything, Bruce. Everything they do is based on Dermasys.

I'm afraid FUM is the very definition of a one trick pony. They centre everything around Dermasys, and mix (or not) other ingredients in with it to deliver medication through the skin. As they say themselves, " What we do. Our technology.
Our core strength lies in our research and development capabilities in the field of topical formulations and transdermal delivery."

Volat1lity, damn right they would have discussed FM57, but only in regards to MED3000 being the placebo rather than the subject of the trial, which is how FUM are trying to represent it now. MED3000 has never been subject to any kind of trial per se, and the FDA and probably EMA require it.