Geron no follow through

No follow through from Thursday's  +3 million shares. Friday's close was $2.56 down 2 cent from Thursday's close. Volume was only 1,392,000. The five day avg was 1,476,060, ten days avg was 1,291,355, three month avg 1,664,870. The high was $2.60 on Friday the low was Wed. $2.20. Hoping for some good news from "Chip" the new CEO, Nov 4th Conference Call to discuss third quarter financial results and highlights. We are above the 50 day moving avg of $2.30, the 200 day moving avg is $3.54.

Good luck in this rigged casino,

No Follow Through Geron

No follow through today, price down, no increase in volume, no good news was leaked out. I still think "Chip" will throw us a bone Nov 4th. I will be listening.

Good luck in this rigged casino,

3 Million Shares Traded

Geron traded 3,037,729 shares today closed at $2.58 up 30 cent or 13%. This is very good, volume with price increase.  If we get follow through Friday say 3.5 million shares and a 20 cent price gain, then maybe we have good news coming that will drive the share price even higher. Remember this is why "Chip" was hired as CEO, too get the share price up and get some deals made. Again if we hit $3, I will sell a few covered called.

Good luck in this rigged casino,

Moving up with Market

Geron is moving up big  8.7% to $2.48. But no increase in volume, we've been through this before. If the volume is not over 2 million today I'm not going to get to excited. With "Chip" the new CEO running the the show now, we could get some good news at the Nov. 4th Conference. Increase in volume with a share price rise is the best sign that some thing good is around the corner. Any move to $3, I will sell a few covered calls.

Good luck in this rigged casino.

Geron the next big thing

For over ten years the leadership was all about the science. Now we have drugs that are products of that science. Geron hires "Chip" as CEO. The man who has a proven track record for making investors money. I see Geron becoming the next big thing. Bigger then AAPL, GOOG or any pharma company. It might take 20 more years but Geron could do it. Always remember you can lose all your money in any stock.

Good luck in this rigged casino,

Right now the fifth patient is being evaluated for GRNOPC1

Right now the fifth patient is being evaluated, for GRNOPC1 phase one trial using stem cells to treat patients with spinal cord injuries.

This is not the time to sell at $2.00. This company could be $25.00 overnight if one of the test patients shows movement. Or if big pharma takes a position $8.00 is possible.

I think a sustainable big jump will take place some time in late spring 2012, when some kind of deal is leaked out and confirmed later. I believe "Chip" is busy doing that job right now.

Good luck in this rigged casino,

Geron announces Conference Call for Third Quarter

Geron Announces Conference Call to Discuss Third Quarter Financial Results and Highlights. November 4, 2011 at 9AM Eastern Time. Dial 1-800-706-7748 the passcode is 53572623.

More good data from GRNOPC1

Oct 25, 2011 07:31:09 (ET)

MENLO PARK, Calif., Oct 25, 2011 (BUSINESS WIRE) -- Geron Corporation (GERN, Trade)
today announced data on the use of GRNOPC1, oligodendrocyte progenitors derived from
 human embryonic stem cells, for myelin repair in a non-human primate model. The data supports
 further investigation of the potential therapeutic use of GRNOPC1 in central nervous system
(CNS) disorders where the central or contributing pathology is destructive removal of myelin
 from nerve axons, such as observed in multiple sclerosis (MS), myelitis and spinal cord injury.
 GRNOPC1 is currently in a Phase 1 clinical trial in patients with spinal cord injury.The new
data were presented at the 5th Joint Triennial Congress of the European and Americas Committees
 for Treatment and Research in Multiple Sclerosis, in Amsterdam, by Prof. Jeffery D. Kocsis,
 Ph.D., from Yale University School of Medicine. The work was performed in collaboration
with scientists at Geron.
The studies utilized a non-human primate model where demyelinated lesions, such as seen
in multiple sclerosis, were induced chemically in the spinal cord. GRNOPC1 was injected
 into the demyelinated spinal cord lesions one week after chemical induction. The lesion sites
 from six monkeys were analyzed using light and electron microscopy at various timepoints
 up to one year after injection of GRNOPC1 to look for evidence of cell survival and
remyelination of nerve axons. In the first few weeks  after implantation, the injection sites
contained maturing transplanted cells indicative of a premyelinating phenotype with evidence
 of variable numbers and degrees of remyelinated axons. By four months post implantation,
GRNOPC1 had induced extensive and thick myelin around the formerly denuded axons.
Human cells were detected at the lesion site, providing evidence for survival of
 transplanted GRNOPC1. There was no evidence of abnormal tissue, tumor formation or
other pathologies associated with the injection of GRNOPC1. Neurological exams of the injected
 animals were normal. The data showed in the non-human primate that GRNOPC1 can survive
 at the lesion site and progressively remyelination of axons. "These new data confirm and
extend previous results showing that GRNOPC1 can promote remyelination in rodents and
 non-human primates," said Jane Lebkowski, Ph.D., Geron's Chief Scientific Officer. "These
 results provide  further support for the potential of GRNOPC1 to provide therapeutic
benefit in a number of central nervous system diseases, such as MS and myelitis."
About GRNOPC1
Oligodendrocytes produce myelin, an insulating layer made up of protein and fatty substances
 that forms around nerves in the CNS to enable them to conduct electrical signals. Without
 myelin, many of the nerves in the brain and spinal cord cannot function properly. Oligodendrocytes
 are lost in CNS disorders such as spinal cord injury and MS.
GRNOPC1 contains hESC-derived oligodendrocyte progenitor cells that have demonstrated
remyelinating, nerve growth stimulating and angiogenic properties leading to restoration
 of function in rodent models of acute spinal cord  injury. Non-clinical studies have shown that 

administration of GRNOPC1 seven days after injury significantly improved locomotor activity
and kinematic scores of rats with spinal
About Geron
Geron is developing first-in-class biopharmaceuticals for the treatment of cancer and chronic
degenerative diseases. The company is advancing anti-cancer therapies through multiple
Phase 2 clinical trials in different cancers by targeting the enzyme telomerase and
 with a compound designed to penetrate the blood-brain barrier. The company is developing
 cell therapies from differentiated human embryonic stem cells, with the first product in a
Phase 1 clinical trial for spinal cord injury.
 For more information, visit www.geron.com .

Safety data on GRNOPC1

Safety data to data form the trial has shown:

1.No surgical complications during or after the procedures.
2.No adverse events related to the injection procedures or to GRNOPC1.
3.A few mild adverse events related to tacrolimus.
4.No evidence of cavitation in the spinal cord at the injury sites on MRI.
5.No unexpected neurological changes.
6.No evidence of immune responses to GRNOPC1.

GRNOPC1 was delivered to four spinal cord injured patients at a dose of two million cells without complications from either the cells or the surgical procedure itself, and without any negative effects on the spinal cord or neurological function of the patients to date. The only side-effects observed were due to the immunosuppressive drug tacrolimus, which is administered for the first two months after injection of GRNOPC1. Furthermore, there is no evidence to date of immune rejection of GRNOPC1, an allogeneic cell therapy, including after withdrawal of immunosuppressive drug.
The facts all point to success. We know that these stem cells work. The big question is whether they are safe. We have shown that to date.  Geron is positioned for huge increases from this and Oncology programs. Then orchestrated takeover bid most likely scenario, as any review of the new CEO will indicate. Those are the facts.  Stock moves up. Market as well.


Good luck in this rigged casino,

No Interest

Five day avg volume only 1,084,860 shares, ten day avg. 1,281,746 and three month avg. 1,651,130 shares. Market has no real interest in Geron at this time. The high for the week was $2.38 on Monday and low was $2.11 on Wednesday. Share price has been range bound from Sept 22-Oct 21,  between $1.87 to $2.38. Only under $2, two days and closed over $2 on those days. Will be buying more on any dips close to $2.

Good luck in this rigged casino,

GERON the future in bio-tech: Manipulation

GERON the future in bio-tech: Manipulation: Yes, manipulation of share price does happen and is happening. If we get a toe wiggle or the results from the four Phase 2 cancer drug appe...

Manipulation

Yes, manipulation of share price does happen and is happening. If we get a toe wiggle or the results from the four Phase 2 cancer drug appears to be successful none of the Market Makers, hedge funds or institutions will be capable of stopping the huge run up.  The market is bigger then any Market Maker or hedge fund.  When things are in doubt, fear can be planted and exploited.  The Market Makers, hedge funds and institutions will take advantage. They cover, they switch sides but they are not stupid enough to try an stop a big move up. If you believe like I do buy a few shares on the dips. Many are shorting and or are selling, when they should be accumulating.  Always, Always remember to can lose all your money in any stock.

Good luck in this rigged casino,

Geron Q and A Dr. Gold

Dr.Gold, "So far 4 patients have been treated, It was never our intent to publicize their identities or their progress. The first patient was treated a year ago. No adverse effects whatsoever, which was the goal, because it allows us to ramp up the dose from a "safety" range to a "beneficial function" range. Going forward, there will be cervical patients, higher doses, and efforts to break up the scar tissue so that whatever works in subacutes also helps chronics."
Then Q and A
Q: Dr Gold, please tell us something about the patients you've treated at Geron.
A: No, I'm not allowed to talk about that. I do need to say that we'd be delighted, of course.
This is good news, Geron is moving forward. With some luck we might get a toe wiggle. If not now, later with the higher doses.
Good luck in this rigged casino,

Data Update on GRNOPC1 spinal cord injury

Oct 20, 2011 07:30:02 (ET)

MENLO PARK, Calif., Oct 20, 2011 (BUSINESS WIRE) -- Geron Corporation (GERN, Trade )
 today announced two presentations on the company's ongoing Phase 1 clinical trial of its human
 embryonic stem cell-based therapy, GRNOPC1, in patients with spinal cord injury. Safety data
were presented at the Pre-Conference Symposia of the joint 2011 American Congress of
Rehabilitation Medicine and American Society of Neuro-Radiology Annual Meeting in Atlanta,
GA. A second presentation was given at the Working 2 Walk 2011 conference in Rockville,
MD. The presentations were given by Joseph Gold, Ph.D., Geron's Senior Director of
Neurobiology and Stem Cell Therapies and Linda Jones, P.T., M.S., Geron's Senior Clinical
Trials Manager for GRNOPC1. "We are pleased to report that the lowest intended dose of
 GRNOPC1 has been administered to four patients with complete thoracic spinal cord injuries,"
 said Stephen M. Kelsey, M.D., Geron's Head of Research & Development and Chief Medical
 Officer. "To date, GRNOPC1 has been well tolerated with no serious adverse events."
Phase 1 Clinical Trial Data
Data were presented on four patients with neurologically complete American Spinal Injury Association
(ASIA) Impairment Scale grade A thoracic spinal cord injuries, who received GRNOPC1 at a dose of
two million cells delivered by injection into the lesion site using a syringe positioning device designed by
 Geron. GRNOPC1 was administered between 7 and 14 days after injury. Low-dose tacrolimus was
 given for temporary immune-suppression from the time of injection for 46 days, at which point the dose
was tapered and withdrawn completely at 60 days.
Endpoints of the trial are safety and evaluation of neurological function, using standardized testing at
specified timepoints to monitor sensory and lower extremity motor function. The trial protocol also includes
 multiple MRI scans. Initial follow-up of patients is one year. One patient in the trial has completed the
Day 365 follow-up visit. The most recent patient to be enrolled in the clinical trial has completed the Day
30 follow-up. After one year the patients enter a period of long-term follow-up that includes annual in-
person visits for the first five years and subsequent yearly check-ups via telephone for an additional nine
years.
Safety data to date from the trial has shown:
-- No surgical complications during or after the procedures.
-- No adverse events related to the injection procedures or to GRNOPC1.
-- A few mild adverse events related to tacrolimus.
-- No evidence of cavitation in the spinal cord at the injury sites on MRI.
-- No unexpected neurological changes.
-- No evidence of immune responses to GRNOPC1.
GRNOPC1 was delivered to four spinal cord injured patients at a dose of two million cells without
complications from either the cells or the surgical procedure itself, and without any negative effects on
 the spinal cord or neurological function of the patients to date. The only side-effects observed were due
 to the immunosuppressive drug tacrolimus, which is administered for the first two months after injection
of GRNOPC1. Furthermore, there is no evidence to date of immune rejection of GRNOPC1, an allogeneic
 cell therapy, including after withdrawal of immunosuppressive drug.
About GRNOPC1
GRNOPC1 contains hESC-derived oligodendrocyte progenitor cells that have demonstrated remyelinating
, nerve growth stimulating and angiogenic properties leading to restoration of function in rodent models of
acute spinal cord injury. Preclinical studies have shown that administration of GRNOPC1 significantly
improved locomotor activity and kinematic scores of rodents with spinal cord injuries when injected seven
days after the injury. Histological examination of the injured spinal cords treated with GRNOPC1 showed
 improved axon survival and extensive remyelination surrounding the rodent axons. For more information
 about GRNOPC1, visit www.geron.com/GRNOPC1Trial/ . For further information about the Phase 1
clinical trial, including location of clinical sites, visit http://clinicaltrials.gov/ct2/show/NCT01217008 .
About Spinal Cord Injury
Spinal cord injury is caused by trauma to the spinal cord that results in a loss of motor control, sensatory
 perception, bowel and bladder control, and numerous other voluntary or involuntary body functions. A
 traumatic blow to the spine can fracture or dislocate vertebrae that may cause bone fragments or disc
material to injure the nerve fibers and damage the oligodendrocyte cells that insulate the nerve fibers in the
 spinal cord. Most human spinal cord injuries are contusions (bruises) rather than lacerations to the cord.
 Every year approximately 12,000 people in the U.S. sustain spinal cord injuries. There are currently no
approved therapies for the treatment of spinal cord injury.
About Geron
Geron is developing first-in-class biopharmaceuticals for the treatment of cancer and chronic degenerative
 diseases. The company is advancing anti-cancer therapies through multiple Phase 2 clinical trials in
different cancers by targeting the enzyme telomerase and with a compound designed to penetrate the
 blood-brain barrier. The company is developing cell therapies from differentiated human embryonic stem
 cells for a range of indications, with the first product in a Phase 1 clinical trial for spinal cord injury. For
 more information, visit www.geron.com .
This news release may contain forward-looking statements made pursuant to the "safe harbor" provisions
 of the Private Securities Litigation Reform Act of 1995. Investors are cautioned that statements in this
 press release regarding potential applications of Geron's human embryonic stem cell technologies and
 GRNOPC1 constitute forward-looking statements that involve risks and uncertainties, including, without
 limitation, risks inherent in the development and commercialization of potential products, uncertainty of
clinical trial results or regulatory approvals or clearances, need for future capital, dependence upon
collaborators and protection of our intellectual property rights. Actual results may differ materially from the
 results anticipated in these forward-looking statements. Additional information on potential factors that
 could affect our results and other risks and uncertainties are detailed from time to time in Geron's periodic
reports, filed with the Securities and Exchange Commission, including the quarterly report on Form 10-Q
 for the quarter ended June 30, 2011.
SOURCE: Geron Corporation

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Viacyte Case Geron share price will rise

I'm not going into detail on Geron suing Viacyte over patent infringement. It looks like Geron may win. The lawyer at Geron buys 50,000 shares in early Oct. Indicates that the case is going in Geron favor.

Remember the new CEO who has a history of selling to big pharma every time he takes over a new company.
The European court ruling today, Geron benefits with other U.S. based stem cell companies.

Geron price rises and or Geron gets bought out, not the whole company but pieces.

Will be buying more shares and selling cover calls on any price spike. Also will sell a few shares on any price spike.

Geron's Goals for 2012

Regulatory acceptance for OPC1 SC1 thoracic dose escalation Q1/2012

Regulatory acceptance for OPC1 SC1 cervical cohort Q1/2012

Declaration of IND Candidacy for GRN510 Q1/2012

PFS data in imetelstat Phase 2 in NSCLC Q2/2012

PFS data in imetelstat Phase 2 in Breast Cancer Q2/2012

ORR data in imetelstat Phase 2 in Multiple Myeloma Q2/2012

Hematologic response rate in imetelstat Phase 2 in ET Q2/2012

ORR data GRN1005 NSCLC brain mets Phase 2 Q4/2012

ORR data GRN1005 Breast Cancer brain mets Phase 2 Q4/2012.
2012 will be a very important year for Geron. With a new CEO who is a deal maker. The four phase 2 trials ending in Dec of 2012 and results will be reported then. I'm hoping for a $5 to $10 share price.  I will be buying a few more shares on the dips and will sell a few shares and or sell some covered calls on the rips up.

Good luck in this rigged casino,

Geron initiate randomized Phase 2 in Breast Cancer

Oct 14th Geron initiates randomized Phase 2 clinical trial of imetelstat in breast cancer. Enrollment of the first patient using a telomerase inhibitor drug GRN163L. The results will be known the end of 2012.

The high for the was on Wed. Oct 12th of $2.38, the low of $2.18 was on Mon. Oct 10th. The avg. volume is going down. The one year update on Oct 16th, on there Phase 1 GRNOPC1 looks like no great news. I'm basing this on no increase in volume or price. I hope I'm wrong.

Good luck in this rigged casino,

Update on Phase 1 GRNOPC1 Spinal Cord injuries

U2FP, Working 2 Walk, Oct 16th at 9:45AM at Hilton Rockville, Washington D.C.  Joseph Gold PhD Senior Director at Geron will give a update on Phase 1 Safety Trial of Human Embryonic Stem-Cell GRNOPC1 in subjects with neurologically complete, subacute spinal cord injuries. Geron is up 5% I think people are hoping for good news Sunday. The volume is not there, yet. Will sell some puts if we get to $3 before the Oct 16th update. If there is an increase in volume say 2 million+ shares a day before update I will not sell puts.

Good luck in this rigged casino,

Geron and ACTC leading the stem cell revolution

This is from Michael J. Ray's blog on Seeking Alpha. I'm long both Geron and ACTC.

 One cannot initiate a discussion of stem cell companies without starting with Geron (GERN). Geron is a company that develops biopharmaceuticals for the treatment of cancer and chronic degenerative diseases, including spinal cord injury, heart failure, and diabetes. GERN’s pipelines run fairly deep and besides stem cell technologies it has multiple Phase 2 trials dealing with cancer therapies. That being the case, the real catalyst for the company is the Phase 1 clinical trial dealing with treatment of spinal cord injuries with stem cells. If GERN is going to be the catalyst that starts this medical revolution then it will begin in this trial.

paralysis in many patients. In animal models, Geron was able to show improved functional behavior using GRNOPC1 at the injury site seven days after injury. After much review, the FDA then granted approval for a clinical trial and Phase 1 testing of GRNOPC1 in patients with spinal cord injury began in October 2010. Two clinical sites were opened for patient enrollment in 2010, and the remaining 5 were opened in 2011.

What GERN has done is to derived Oligodendrocyte progenitor cells (GRNOPC1) from Human Embryonic Stem Cell (hESCs). Oligodendrocytes are naturally occurring cells in the nervous system that have several functions. They produce myelin (insulating layers of cell membrane) that enables the cells to conduct electrical impulses, plus they also produce neurotrophic factors that support the maintenance of nerve cells. When these Oligodendrocytes are lost in spinal cord injuries, the results are a loss of the myelin and neuronal function that in the end will cause 

In late July 2011, Geron stated that a second subject was enrolled and received GRNOPC1 in the ongoing Phase 1 clinical trial. The treatment was administered by investigators at Northwestern Memorial Hospital and Northwestern University Feinberg School of Medicine. The company also went on to state that the preliminary data from the first two patients showed no safety concerns or serious adverse events. That being the case, Geron received clearance from the FDA to expand the eligibility criteria for the trial to allow inclusion of a wider range of patients.

million. The company also stated that the cash reserve plus the income Geron receives will be sufficient to fund the current level of operations through at least December 2012. Geron also states that future capital requirements will be substantial as several trials are moving forward.

For the second quarter of 2011, the company reported a net loss of $21.1 million. Net loss for the first six months of 2011 was $45.5 million and the company ended the quarter with $192.2 million in cash and investments. The total operating expenses for the second quarter of 2011 were $21.9 million which broke down to research and development expenses of $16.5 million and general and administrative expenses of $5.3 

So will Geron be the one who will strike first with its stem cell therapy? Phase 1 trials have been going on for awhile and so far all we have really heard is that the therapies are safe but we are still unsure as to how effective they are. It is obvious that the trial is very ambitious and if successful will be a game changer, but one must worry if the company will run out of funding before they get to that point. It will be most interesting to watch as events unfold in this company’s future.

commercialization of human embryonic and adult stem cell technology in the field of regenerative medicine. In early 2010 the FDA granted orphan drug status to Advanced Cell for an embryonic stem cell derived treatment for a specific form of blindness, Stargardt’s Macular Dystrophy.

If Geron is not moving at the pace you want, then you might want to consider fast acting Advanced Cell Technology (ACTC). Advanced Cell is a biotechnology company focused on the development and 

Later that same year the company was cleared by U.S. regulators to test a therapy made from embryonic stem cells in patients with macular degeneration. Advanced Cell wasted little time and by July 2011 the company announced the dosing of the first patients in each of its two Phase 1/2 clinical trials for Stargardt's macular dystrophy and dry age-related macular degeneration (dry AMD). These patients were treated at the David Geffen School of Medicine at UCLA and at UCLA's Jules Stein Eye Institute. Notice that the trial is Phase1/2 thereby speeding up the trials. Both the Stargardt's trial and the dry AMD trial will enroll 12 patients each, with cohorts of three patients each receiving an ascending dosage of the stem cells as the trials move forward. The initial dosing was relatively small (50,000 cells) and the early indications were that the patients tolerated the surgical procedures well. In late September 2011, the independent Data and Safety Monitoring Board (DSMB) overseeing the Company’s two trials authorized ACTC to move forward with enrolling and treating the next set of patients in each of the trials.

what is going on in Europe. At the same time the DSMB made its announcement, Advanced Cell received clearance from the U.K. Medicines and Healthcare products Regulatory Agency to begin similar Phase 1/2 clinical trial for Stargardt’s Macular Dystrophy. It should also be known that the European Medicines Agency previously granted Orphan Drug designation for the company's RPE cell product for use in treating SMD. At this point it should be noted that macular degeneration in the U.S. is a $30 billion market with relatively no competition. Add a European market to the mix and the numbers go even higher. To add fuel to the fire one has to consider a recent statement from the CEO when he stated,What should be taken away from this is that the pre-clinical animal findings were extremely successful and if this carries forward in humans then the sky is the limit for the company. Also this is the first time that any testing in Asia had been mentioned. And if all that is not enough, one must also consider the Advanced Cell’s Phase II-approved Myoblast autologous adult stem cell therapy for the treatment of chronic heart failure advanced cardiac disease, myocardial infarction, and ischemia; as well as the Hemangioblast (HG) program for the treatment of blood and cardiovascular diseases which is currently in preclinical development.

If that was not enough, then on top of the U.S. trials one must consider 

As wonderful as all Advanced Cell’s programs sound, there are still lots of risks with the company. The company basically has no revenue and for the second quarter of 2011; net cash used in operations was $3.2 million. Needless to say the expenses will only increase as the company pushes forward on its clinical trials. Advanced Cell ended the 2011 second quarter with cash and cash equivalents of $16.1 million and will burn through that rather quickly. Add to this a couple newly filed lawsuits and a 1.7 billion share count and we find Advanced Cell in a race for funding. Advanced Cell has stated that several top pharmaceutical companies are closely following the trials and if the company can prove it can eliminate macular degeneration, it is almost certain it will get a joint venture or even a buyout. Until such time though, investors will have to wait and see if this company will be the spark that lights the fires of stem cell revolution.

For now, it will have to suffice to say that we are extremely pleased and believe that these trials will validate our earlier pre-clinical findings. In the meantime, we have begun to set our sights on expanding our clinical trials to in Europe, having been recently approved to begin our SMD trial in the United Kingdom, and various countries in Asia.

                                     Good luck in this rigged casino,

Stem cell treatment for Spinal Cord Injury has Man moving toes

Unfortunately it's not Geron's treatment, but at Beijing Puhua International Hospital. The treatment was on Osama, age 33, male from Libya. The treatment was four neural stem cell injections via lumbar puncture, self stem cell activation and proliferation program, physical therapy and TCM. Out of all that I only understood the physical therapy part. Improvement was made with his sensation and his movements of his toes. Before the therapy he had no sensation or desire for his urination and could not control it. After the treatment he has a sensation when he is urinating and can control 50%. This story should be good for Geron. It's the same science. Geron needs to get the FDA to raise the number of stem cell to 10 million at least. Now it's only 2 million stem cell. Geron should see results like Osama had with an increased dose. With any luck Geron should get it raise by 2nd Q of 2012.

Good luck in this rigged casino,

Geron week in review

The high for the week was $2.24 on Friday Oct. 7. A new 52 week low of $1.87 on Tuesday Oct. 4. The five day avg volume was 1,845,680 shares, ten day avg volume was 1,625,772 shares and the three month avg volume was 1,626,447. The low is in for now. With the new CEO "Chip" we should move higher. He's a deal maker and we need money.  The inside buyer of 50,000 shares on Oct 5 at $2.03 a share was a very good sign.
Better days are coming for Geron.

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Inside buying Geron

Kiley Thomas Director at Geron bought 50,000 shares on Oct. 5, 2011 at $2.03 a share. This is a very good sign. No one is going to buy $100,000 worth of stock in a company, they don't believe will make it big time. We need more inside buying like this. I now have 9,600+ shares, if Geron does not make it big, I will be working till I'm 70+.
A one year update on TJ would be nice. TJ was the first person injected with GRNOPC1 in Oct of 2010, using stem cells to treat patients with spinal cord injuries.

Good luck in this rigged casino,

Who are selling Geron under $2

Only the Scaredy-Cats, who have no business investing. Geron has a cash position of about $1.60 per share and a IP portfolio that has a potential value in the 100's of billions of dollars. If only one of the four platforms work out, the Longs will be very rich. The four platforms are GRNOPC1, GRN163L, GRN1005 and the drug toxicity platform. This is real, nothing has changed except for the management. "Chip" the new CEO is a big plus and will be making deals that will bring cash to Geron. Do your own research there is serious value here. The current price barely covers the cash on hand. If you are a True Believer like myself, buy a few more shares. I did at $1.95. We will be rewarded. A blockbuster is just around he corner. Always remember you can lose all your money in any stock.

Good luck in this rigged casino,

Going down

The whole market is going down. Geron will break under $2. If you believe in Geron buy a few shares. The people are running scared. Buy the whole market like SPY, DIA, IYY, QQQQ, Market way over sold.

The true believers will be buying. Always remember you can lose all your money in any stock.

Good luck in this rigged casino,

New 52 week low

I added more shares at $2.01. I feel Geron is at the bottom, I thought that at $2.09. If the market goes down more so will Geron. Only a good news story will stop it. If you believe in Geron buy a few shares. Things will get better and Geron will go above $3.00. Remember you can lose all your money in any stock. I'm doing a great job losing mind. True believers start buying.

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Geron bottom in

Geron has so many positives. The science, money in the bank and now a CEO that is a true businessman famous for making deals. Geron will sell some parts, will have partners and will develop some products. The main thing the days of secondaries are over [at under $10]. I added a few more shares today at $2.09. Remember you can lose all your money on any stock.

Good luck in this rigged casino,

Share price will rise

2012 will be a very important year for Geron. With a new CEO who is a deal maker. The share price should go higher. The four phase two trials end in Dec of 2012 and results will be reported then. The GRN 1005 will be in phase two soon if that trial goes well it could get fast tracked. GRNOPC1 in phase one trial, using stem cells to treat patients with spinal cord injuries, any good results would send the share price to the moon. I've been buying all the way down from $4 to $2 avg share price is now $3.80. I will sell a few shares on big prices moves.

Good luck in this rigged casino,
Lee