In Contact with SEC
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I don't know why ,but I busted up laughing reading this..tell them off for all of us !
Tell them us shareholders will be suing them and then ask them how they feel about that..not too good, I would imagine.
Thanks !
Yep, let's break the 2's and work up to the 3's !
Good Morning ,been a long weekend !
Accelerated Approval Requires .....
"In some cases the Phase II studies reveal results so impressive that these studies alone are the basis for approval, generally for treatment of refractory disease. This is often done under FDA's accelerated approval rule (similar to the fast-track provision under FDA's Modernization Act of 1997 [FDAMA]) which allows FDA to approve drugs on the basis of a surrogate endpoint (effect on a measurement such as a tumor size likely to lead to a real patient improvement) on condition that post-marketing studies demonstrate a tangible patient benefit. In most cases, if Phase II studies show desirable responses, Phase III studies are conducted. Those are concurrently controlled studies in which two therapies are compared. These usually are 1) a comparison of standard treatment alone, or 2) a comparison of the new treatment alone with an older treatment to show that the new treatment is not worse than the older treatment or is its superior."
http://www.fda.gov/NewsEvents/Testimony/ucm115209.htm
We haven't started Phase 1
Phase 1 and phase 2 need to be completed for any Accelerated Approval.
While that's great ....I wonder how many shares there were being they bought the entire 100% .
$160 million really isn't a lot. Say we have 160 million shares..do the math.
The cost of the patents is around 13% of $160 million alone.
SBFM would need a HUGE buy out .
Just throwing $ scenarios out here.
January effect....
https://www.peterleeds.com/blog.htm?blog=538/
January effect....
https://www.peterleeds.com/blog.htm?blog=538/
Accelerated Approval Requires .....
"In some cases the Phase II studies reveal results so impressive that these studies alone are the basis for approval, generally for treatment of refractory disease. This is often done under FDA's accelerated approval rule (similar to the fast-track provision under FDA's Modernization Act of 1997 [FDAMA]) which allows FDA to approve drugs on the basis of a surrogate endpoint (effect on a measurement such as a tumor size likely to lead to a real patient improvement) on condition that post-marketing studies demonstrate a tangible patient benefit. In most cases, if Phase II studies show desirable responses, Phase III studies are conducted. Those are concurrently controlled studies in which two therapies are compared. These usually are 1) a comparison of standard treatment alone, or 2) a comparison of the new treatment alone with an older treatment to show that the new treatment is not worse than the older treatment or is its superior."
http://www.fda.gov/NewsEvents/Testimony/ucm115209.htm
We haven't even started Phase 1
Phase 1 and phase 2 need to be completed for any Accelerated Approval.
I been researching "Jewish General Hospital in Montreal (Canada)" and they are mainly a teaching school ,but do tons of research and clinical trials.
I'm currently looking to see if there's any mention of any clinical trials regarding "Adva-27a for Pancreatic Cancer and Breast Cancer"
If I can't find anything ,it doesn't mean it's not going to happen.
This link took me to the next link and currently going thru their archive of clinical trials. Anyone want to hop in and look ,go right ahead.
I don't think I will find anything ,because phase 1 trials haven't started as of yet,but I'll look anyway.
http://www.jgh.ca/en/LDI?mid=ctl00_MainMenu_ctl00_TheMenu-menuItem007
http://www.ladydavis.ca/
They do have an excellent record and is one of Canada's leading health research institutes.
"The Lady Davis Institute (LDI) is the research arm of Montreal's Jewish General Hospital, a teaching hospital of McGill University.
Founded in 1969, the LDI is one of Canada's leading health research institutes. Important discoveries which have contributed to the health and well-being of patients in Quebec, Canada, and around the world, have been made by LDI researchers in the areas of HIV/AIDS, aging, cancer, vascular disease, epidemiology, and psychosocial science. There are currently more than 117 full-time researchers at the LDI, of whom 70 are primarily lab-based, 21 investigate psychosocial aspects of disease, 26 are in epidemiology. In addition, there are 124 associate investigators."
I figured that and wanted to make sure.
I've been reading all the Fins since 2011 and checking the charts since 2011 along with the PPS since 2011.
They have been ready for phase 1 since 2011
" Plan of Operation : The Company is planning Phase I clinical trials of Adva-27a for Pancreatic Cancer and in parallel Multidrug Resistant Breast Cancer to be conducted at McGill University's Jewish General Hospital in Montreal (Canada)."
http://yahoo.brand.edgar-online.com/displayfilinginfo.aspx?FilingID=8087691-6863-81285&type=sect&TabIndex=2&companyid=746676&ppu=%252fdefault.aspx%253fcik%253d1402328
No pumping or bashing here...I mainly flip the majority of my penny plays and go flat and move on . I don't even post in the ones I flip.
Some of these plays (not many) I hold some free shares after profit taking and go long just in case ,including this one.
If SBFM can creep back up to the price range of Aug 2nd 2011 or around near it ,it would be nice. Thing is , they really need to get phase 1 started ,to move to the next level.
What phase is SBFM at now ?
Make up your mind or stop with the nonsense.
http://investorshub.advfn.com/boards/read_msg.aspx?message_id=118606486
Hmmmm I can no longer respond to private messages and all the other paid services. They were free up to New years day.
I can no longer respond...all free features expired Jan 1st.
I've been loaded up to the gills since the low .ooxx's
That link regarding SBFM says ....
"Disclosure: We own no shares of SBFM and have not been compensated for this article."
I like that this article wasn't bought and paid for by SBFM.
Somebody slap Etrade ask .0189 for 25g shares. Let's see if it pops to .0195 I'm already loaded to the gills.
Let's bust thru .02 and create support there.OH YEAH !
I file complaints with all SEC FINRA AG FBI.
I email them everyday and call as often as possible and once a month I send hand written letters with Symbol and CEO name on back of letter.
This way it's always fresh in their mind.
Haven't done this with TBEV..well not yet...see how it plays out.
I rather a full day..thanks !
Nope 2pm today.
1 hour of trading left for the day.
Stick around..everything goes up and down. There will be profit taking causing dips,just watch the tape for your entry point.
Good luck.
52 week high is 5 cents. Let's do it again !
Want to make money,just do the complete opposite of what he does..lol
You said here in this post you want to short this stock.Why are you lying ?
http://investorshub.advfn.com/boards/read_msg.aspx?message_id=119397910
"admiralH Thursday, 12/24/15 07:44:08 AM
Re: the third leg post# 22689
Post # of 23298
This is all rather weak IMHO.
A company with limited funding and progress (NovaRX) agrees to be bought out by a worthless penny stock and investors are supposed to gamble on this because of the resumes of the board??????? Wow!
First of all, its misguided to think that a board alone can overcome the weaknesses of an operating company. It cannot. The operating company has to have substance first.
Secondly, the valuable companies are going for traditional IPOs and not backing into empty shells with a history of litigation and loss of assets.
I can't wait for the price to go up so I can short it!!!!!!!!!!!!!!"
Good for you.
While I flip the majority of my penny plays, I do have a few lotto stocks that I believe in and VPRO is one of them.
Just be alert and be prepared for anything to happen..after all this is still pennyland.
Go watch some you tube videos on level 2 ,charting and how to screen for stocks. Much easier to understand when seeing it as oppose to just reading about it.
That doesn't mean you shouldn't read any books..do both.
Best wishes .
Oh I see..you just joined and post that you can't wait for it to go up so you can short it,but you claim you aren't bashing it.
Hmmmmmmm
Take heed everyone.
He has nothing positive to offer other than to short it as he/she stated in his /her post.
I'm done with you.
How did you come upon this stock in the last 5 days since joining ?
Majority of the people on this board flip and only keep a few lotto stocks.
If I lose on the lotto stocks I'm still ahead from all my flipping,even after the short term capital gains.
Why your own Investment Philosophy IS "Always Take Profits"
This is penny land ,learn how to trade them ,otherwise you'll be broke .
Exactly...MM's looking to shake the weak hands and then sell them back to them during a run up. Rinse and repeat .
Everyone, Stay strong and long ,if you must take some profit be sure to keep some for the long haul.
Best wishes to all !
Ignore the shorts ,as you can see they have all come out of the wood work.
They can have their little short lived party ,but in the end us longs will win.
Plus most of us longs are still way in the green $$$$$$$$
Hey, I'm curious..how did you find this stock?
You picked a good one for your very first trade..good job !
All the best to you .
This post reads just like a post by "Alias7".
If you're going to bash ,please use your original "Alias7" name.
This way the board knows who they are dealing with.
No need to hide who you are ,or do you have a reason ..do tell !
I wish you all the best and hope you make a bundle $.
Good luck to you now on your first trade and may all your future trades be successful as your first.
Learn as much as you can .
GOODLUCK
Thanks and Happy New Year to you too !
LOL hurry up big boys , get it while it's still cheap !
LOL yes it is ..funny because I was going to say the same thing to you LOL !
YES I agree..here's the best part of my other post...
"However, none of these competitor companies can use molecules similar to ours as they would be infringing our patents"
OH YEAH !