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How controlled was that? SMH
LOL... Your posts say otherwise.
Fantasy is believing that the reason for the SP being down is due to the company.
The real reason is collusive manipulation... you know, by your HF handlers.
Do you think anyone really believes you?
https://www.griproom.com/fun/how-to-spot-fake-comments-on-stock-boards
We all know who's behind the collusive manipulation.
Based on your childish posts, I had you pegged for 13.
You're such a lying little menace, Dennis. He who 'likes' his own posts. LOL
Take your crap back to NWBO.
When one finds himself in a hole, it's best to stop digging.
What a child you are... DennisMenace would be a more fitting handle for you.
I want to know who let the NWBO dog in that crapped all over this board with stupidity.
LOL... you have no clue.
Congratulations... you just grabbed the biggest dickhead award away from Leo!
Now, take your award and scram!
I copied and pasted exactly what you said, dipschit. Fortunately for you, your OT post was deleted.
Take your crap and yourself back to NWBO land. Your OT crap isn't welcome here.
These are your exact words, dipschitt...
I was challenging your stupidity about MC. Duh!
You obviously have no clue when you said MC has nothing to do with O/S.
What a dipschitt you are.
The reality is that's a spin hit piece...
Stay on topic; we were talking AD endpoints.
Say what?
You're spot on, Wolf. Especially this line...
Where do you come up with this nonsense? There has been no change in endpoints... just more detail in the evaluation, plus biomarkers. ORs are also still valid!
From clinicaltrials.gov, last updated 8/21/23... 450
STUDY START (ACTUAL)
2019-10-10
PRIMARY COMPLETION (ESTIMATED)
2024-07-31
STUDY COMPLETION (ESTIMATED)
2024-07-31
ENROLLMENT (ESTIMATED)
450
How would you know? LOL So lame!
You're missing the forest for the trees...
ORs were prespecified, met endpoints, and highlighted IMPROVED responders. FDA will be impressed.
Cog and CDR also met stat. sig. mean score improvements. FDA will be impressed.
Cog and CDR found to be even more significant with p-values < .025. FDA will be even more impressed.
Key biomarkers found to provide objective and measurable effectiveness. FDA will be most intrigued.
Oh... and the safety profile is second to none, easily administered and inexpensive!
Add it all up and it spells... APPROVAL!
OLE becomes the confirmatory trial.
It's working out perfectly for doubling one's position. Tell your handlers THANKS!
You need to look at the most recent FDA guidance. Dr. Jin is correct in the recently PR'd data.
So you can stop trying to spin it negatively.
Your idiocy is beyond belief.
Likewise... ready and waiting.
More FUD spin is all that we expect from you... You have a job to do and I'm sure you're paid very well... in Judas coins.
Appreciate you admitting it's your handlers who control the price...
Ignore you!
I believe Missling stated it based on discussions with, either, the FDA or Dr. Jin... who certainly would know if it's acceptable. It would certainly provide the longitudinal confirmatory data as any other trial would... and will complete next July.
We'll soon receive all the data, including subgroup analysis, and all of this combined will likely be quite compelling to the FDA:
The confirmatory trial (OLE) is already underway... this situation is very likely, as mentioned by Missling.
One has to recognize the attempted spin from these fraudsters.
They DID NOT pivot!
Cog and ADL ORs were significant (per the SAP) to highlight patients who IMPROVED and remain so... no change.
Cog and CDR scores were stat. sig. and remain so...
Further investigation on Cog and CDR identify better results than initially found, with P < .025
The biomarkers discovered were identified back in Dec... and brought to light in the 9/14 PR.
There was no pivot... just additional detailed data... and ALL of this data will be presented to the FDA.
It's not that hard.
Never... never give a FUDster a break.
You're such a blathering idiot. Please stop with your pompous posts.
Jin informed you that your statement is absolutely false...
Ridiculous blather! There was no pivot, just additional detail of the successful results, plus identification of key biomarkers for AA pathway.
Psychotic idiot.
Idiot.