FNMA- In to $20!!!!!! Let's Roll!!!!!!!!
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Looks like we are accumulating here... Only a 20 mil diffrence
These patents are a huge deal, Not sure many know that...
GNTA Is the mover for today & Tomorrow
Bought early for my wife and I just bought another 233431 for myself
Charts are set up to run
Downey "DWNFQ" is the breakout "Q" stock today
I'm with you on that
Downey is the breakout "Q" stock today
Great Post
"GNTA" STRONG HOLD by JAYWALK Research
SEE YOU GUY IN THE EARLY MORNING
same here, this one is a regular. I got 2mil, we need that update. Who knows where the $$$$$$ Going
I like holding some positions like a retirement account and others I buy and sell for play money/Pay the bills. Such as the PFFBQ run Monday, yes, I was there and bought friday @.019 and sold @ .09 (sold a little short of the high) but had a great day
We are showing a bid of .0002 tonight
There was news, I believe on Friday about the buyout, maybe even yesterday, but I'll update you in the next day or so
I have other positions that I Sell & Buy daily, I just have a position on this one and will ride it out. I do on a daily average about $1000-2000 daily, some day's less, so take it for what it is + I operate a Landscape/Storage business.
I watched (2)drug stocks in the last 3 weeks in a similar view go from .10 to .50 over-nite in after market trading/Pre-market trading and then ran to $2.85 in (2) days. They both were bought out by larger company's this last week. I missed those pics because I had gone into a margin call and fell below the daytrader limit. I would have to look back to see which ticker symbols they were...
My other reasons for holding is that the guys doing the research like "JAYWALK" rate this as a strong Hold. Like I said before, research does not happen over nite.
If you think so, go ahead. The rest of us will ride this
I will check with one of my customers to see if these products are being tested at his Hospital, He is the Director of Oncology at a hospital in New Jersey
We will see this tick up, I believe we hit the bottom and it will continue to tick up to .15 in the next 2 weeks, then a break of FDA News will send this stock soaring... Remember, these guys Develope drugs that we need and they have been in the developing stages for many years.
I didn't say anything about Friday, I said very soon
yes
"GNTA" is still a stock that sits until FDA Approval is granted. When granted hang on to your seat. This will be a $3.00 stock in no time. We are not the only investors in on this. Many others have millions invested directly for startup and trials.
I've researched this over the past 6 months or soo, I would say confidently, we are close to lifting off, very soon. so stick with it or you will regret that you were not part of this prize pick. I jumped in today for 300,000 and won't sell until we receive our dividend....
Jeff
i'M FLYING WITH YOU TOMORROW. lOST A LITTLE BIT TODAY BUT HEY, jAYWALK HAS THIS AS A STRONG HOLD. wHO IN THEIR RITE MIND WOULD SELL THIS...
Genta Summarizes Phase 2 Activity and Receives Orphan Drug Designation in Gastric Cancer for Tesetaxel, a Leading Oral Taxane in Clinical Development
8:21a ET January 5, 2009 (Business Wire)
Genta Incorporated (OTCBB: GNTA) announced today that the Company has received notice from the U.S. Food and Drug Administration (FDA) that tesetaxel, the latest addition to Genta's oncology product portfolio, has been granted designation as an "Orphan Drug" for treatment of patients with advanced gastric cancer. Orphan drug status provides for a period of marketing exclusivity, certain tax benefits, and an exemption from certain fees upon submission of a New Drug Application. As a late Phase 2 agent, the Company believes tesetaxel is the leading oral taxane currently in clinical development.
In the completed Phase 2 study, 35 patients with advanced gastric cancer were treated with tesetaxel at doses ranging from 27 to 35 mg/m(2) once every three weeks. All patients had received extensive prior treatment, having failed a combination regimen that included cisplatin plus 5-fluorouracil or Xeloda(R), and all but 2 patients had received a third chemotherapy drug with this regimen. Final intent-to-treat analysis, including all patients enrolled in the study, showed that 5 patients achieved a partial response, 2 patients achieved a partial response unconfirmed by CT scan, and 14 patients achieved stable disease, for an overall major response rate of 20% and a disease-control rate of 60%. The most serious adverse reaction was Grade 3-4 neutropenia, which occurred in 57% of patients. Six patients failed to complete the first course of treatment. Five patients died on study from differing causes that included intestinal perforation, pneumonia, hepatic failure, hemorrhagic shock, and rapid disease progression. One patient withdrew before receiving the first treatment dose.
"These response data for tesetaxel in a critically ill patient population show clinical activity at levels that are at least comparable to studies with other taxanes," said Dr. Raymond P. Warrell, Jr., Genta's Chief Executive Officer. "Based on these data, we have consulted extensively with international experts and will be defining a global registration path for tesetaxel as a 2nd-line treatment for patients with advanced gastric cancer. FDA designation as an Orphan Drug provides important assistance in the clinical development process."
About Tesetaxel
Tesetaxel is a novel, orally absorbed, semi-synthetic taxane that is in the same class of drugs as paclitaxel and docetaxel. However, both prototype agents suffer from serious safety issues, particularly hypersensitivity reactions related to intravenous infusions that are occasionally fatal and that require careful premedication and observation. Other prominent side-effects of this drug class include myelosuppression (low blood counts) and peripheral neuropathy (disabling nerve damage).
With administration as an oral capsule, tesetaxel was developed to maintain the high antitumor activity of the taxane drug class while eliminating infusion reactions, reducing neuropathy, and increasing patient convenience. The oral route also enables development of novel schedules that may expand dosing options when tesetaxel is used alone or in combination with other anticancer drugs. Preclinically, tesetaxel has demonstrated substantially higher activity against cell lines that were resistant to paclitaxel and docetaxel, since acquired resistance is not mediated by the multidrug-resistant p-glycoprotein.
As a late Phase 2 oncology product, tesetaxel has demonstrated anticancer activity in its initial clinical trials, and the drug has not been associated with the severe infusion reactions that are linked with other taxanes. Moreover, unlike other oral taxanes, nerve damage has not been a prominent side effect of tesetaxel. Thus, the drug offers substantial opportunities to improve patient convenience, safety, and anticancer activity. More than 250 patients worldwide have been treated with oral tesetaxel in Phase 1 and Phase 2 clinical trials.
About Genta
Genta Incorporated is a biopharmaceutical company with a diversified product portfolio that is focused on delivering innovative products for the treatment of patients with cancer. Two major programs anchor the Company's research platform: DNA/RNA-based Medicines and Small Molecules. Genasense(R) (oblimersen sodium) Injection is the Company's lead compound from its DNA/RNA Medicines program. Genta is currently recruiting patients to the AGENDA Trial, a global Phase 3 trial of Genasense in patients with advanced melanoma. The leading drug in Genta's Small Molecule program is Ganite(R) (gallium nitrate injection), which the Company is exclusively marketing in the U.S. for treatment of symptomatic patients with cancer related hypercalcemia that is resistant to hydration. The Company has developed G4544, an oral formulation of the active ingredient in Ganite, that has recently entered clinical trials as a potential treatment for diseases associated with accelerated bone loss. The Company is also developing tesetaxel, a novel, orally absorbed, semi-synthetic taxane that is in the same class of drugs as paclitaxel and docetaxel. Ganite and Genasense are available on a "named-patient" basis in countries outside the United States. For more information about Genta, please visit our website at: www.genta.com.
Safe Harbor
This press release may contain forward-looking statements with respect to business conducted by Genta Incorporated. By their nature, forward-looking statements and forecasts involve risks and uncertainties because they relate to events and depend on circumstances that will occur in the future. Such forward-looking statements include those that express plan, anticipation, intent, contingency, goals, targets, or future developments and/or otherwise are not statements of historical fact. The words "potentially", "anticipate", "could", "calls for", and similar expressions also identify forward-looking statements. The Company does not undertake to update any forward-looking statements. Factors that could affect actual results include, without limitation, risks associated with:
-- the Company's ability to obtain necessary regulatory approval for Genasense(R) from the U.S. Food and Drug Administration ("FDA");
-- the safety and efficacy of the Company's products or product candidates;
-- the Company's assessment of its clinical trials;
-- the commencement and completion of clinical trials;
-- the Company's ability to develop, manufacture, license and sell its products or product candidates;
-- the Company's ability to enter into and successfully execute license and collaborative agreements, if any;
-- the adequacy of the Company's capital resources and cash flow projections, the Company's ability to obtain sufficient financing to maintain the Company's planned operations, or the Company's risk of bankruptcy;
-- the adequacy of the Company's patents and proprietary rights;
-- the impact of litigation that has been brought against the Company; and
-- the other risks described under Certain Risks and Uncertainties Related to the Company's Business, as contained in the Company's Annual Report on Form 10-K and Quarterly Report on Form 10-Q.
There are a number of factors that could cause actual results and developments to differ materially. For a discussion of those risks and uncertainties, please see the Company's Annual Report on Form 10-K for 2007 and its most recent quarterly report on Form 10-Q.
SOURCE: Genta Incorporated
Genta Investor Relations 908-286-3980 info@genta.com
"GNTA" EXPLOSION TO HAPPEN SOON
OK GUYS, IT'S NOW TIME TO PUSH THIS BABY BACK UP TO .03 TO END THE DAY
ON THE WAY BACK TO .009
FBTXQ IS BACK ON THE RADAR
i WISH i WOULD HAVE BOUGHT THIS FIVE MINUTES LATER(lol) LOST $166.00 IN 5 MINUTES
GNTA- Rated a strong hold on JAYWALK, lET'S WATCH IT BREAK
OK, Thats Bottom
I'm in for 208450 for the end of day run
I just put my order in 185,957 @ .015
No need to worry about nite today
DWNFQ-Has the money$$$$$$, needs the buys/Volume
We need the volume, It was up.003 on 30,000 volume early
Come on in. need volume to make the run
"DWNFQ" is running to .12 today. Need volume, Let's go guys...
"DWNFQ" running today, small orders now with big returns. Todays our day
Look at the small orders pushing us up, It's our turn