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By Jamie Moye

Within the next three months, certainly before the end of August, some poor soul is going to find himself in the hospital with a broken back, facing a future life as a paraplegic. With essentially no hope of a cure from currently available medical treatments, this individual will agree to participate in a groundbreaking new clinical study that could help heal his devastating injury and usher in a whole new paradigm of medical treatment for a variety of illnesses and injuries.

Geron Corp. (GERN) is the first company to receive U.S. Food and Drug Administration (FDA) clearance for the world’s first clinical study of a human embryonic stem cell (hESC)-based therapy in humans. The phase I trial is primarily designed to demonstrate the safety of GERN’s GRNOPC1 in patients with “complete” American Spinal Injury Association (ASIA) grade A subacute thoracic spinal cord injuries (essentially a severance of the spinal cord resulting in complete loss of motor and sensory function below the break). However, if that first recipient of GRNOPC1 starts wiggling his proverbial toes the world’s entire medical community, as well as Wall Street, will take notice.

Such a toe wiggle would undoubtedly spark a large spike in GERN’s share price (currently at about $7), which would likely be followed by extreme volatility for months, if not years, to come as GRNOPC1 winds its way through the FDA approval process, and investors mark every toe wiggle, as well as any hint of a possible side affect or bureaucratic delay.

Will we see a toe wiggle?

Preclinical evidence as highlighted in GERN’s 21,000 page FDA Investigational New Drug application suggests that we will, as numerous animal studies demonstrated “significantly improved locomotor activity and kinematic (movement) scores” after treatment. And if thousands of rats with broken backs were able to wriggle their toes and more after being injected by GRNOPC1, it would seem likely that a similar response will be seen in humans. The animal studies also demonstrated no evidence of toxicity, tumor formation or mortality in the receiving animals.

So, what is GERN worth?

Right now, about $7.

OK, so what is GERN worth if GRNOPC1 works?

“Priceless” would argue the 50,000 or so people worldwide who suffer crippling spinal cord injuries every year.

“Nothing without FDA approval” would argue Wall Street.

All right, what is GERN worth with an FDA approval of GRNOPC1?

To date, the company has not offered up any plans for how much it might charge each patient for the treatment, and part of the answer probably lies in how patients fare in the clinical studies–i.e., what level of motor and sensory function return patients gain from the treatment. Thus any effort to put a treatment cost on GRNOPC1 would be a stab in the dark, but given that there are no current medical options for severe spinal cord injuries, the price will undoubtedly be high.

Let’s turn out the lights and throw a knife or two: The average cost of repairing badly torn knee cartilage averages about $12,000 and the costs of repairing a broken heart can soar far above $100,000. Fixing a broken back is certainly worth more than fixing a knee, but may not be as valuable as fixing a heart (that is unless you’re considering this while pondering life in a wheelchair).

So, at the potential low end of the scale, Gern’s treatment might warrant a cost of $30,000 per patient. Using this figure, and estimating that a conservative 50 percent of spinal cord injured patients opt for the treatment, would result in annual revenues of $750 million. Up the treatment cost to the higher end of the scale, at say $60,000, annual revenues with 50 percent of the potential patients would be $1.5 billion. Not too shabby for a company with a current market cap of about $600 million.

If GRNOPC1 shows promise early on then it could receive fast-track designation by FDA and see approval as early as 2012. By using a 6X sales ratio to the conservative $750 million revenue projection, we obtain a valuation of $4.5 billion, or about $50 per share. By using the less conservative $1.5 billion in revenues, we can get a valuation of $9 billion, or about $100 per share.

But the Geron story doesn’t end with GRNOPC1, as the company has numerous other therapeutic products under development.

In the hESC field GERN is also actively studying the use of stem cells for the treatment of heart disease, Type 1 Diabetes, Osteoporosis and Osteoarthritis.

GERN’s heart disease treatment, GRNCM1, is furthest along in the pipeline, and undergoing preclinical studies in animals. The stem cells are designed to replace damaged heart cells and and grow into healthy heart muscle tissue. The approach has been demonstrated in mice, in which stem cells were injected into mice hearts and successfully engrafted and improved the left ventricular function. The company is currently conducting preclinical testing in larger animals.

The company has successfully derived insulin-producing cells from stem cells and injected them into diabetic mice, which demonstrated a response to high levels of glucose in their blood and extended their survival. Small animal studies are continuing.

GERN’s research into developing stem cell therapies for Osteoporosis and Osteoarthritis is in the initial stages of small animal testing and further advancement of these products will depend on how well the treatments work in repairing bone and cartilage damage.

Along with being the leader in the stem cell therapeutic arena, GERN is the leading biopharmaceutical company in the development of cancer-fighting therapies based on telomerase. Telomeres, located on the ends of chromosomes, act as “molecular clocks” for cells, and the human enzyme telomerase can reset these clocks. While not a cause of cancer, GERN and other researchers determined that telomerase is abnormally activated in all cancer types, allowing cancer cells to replicate indefinitely and thereby enable tumor growth and metastasis. But the researchers also discovered that inhibiting telomerase activity can kill cancer cells.

GERN has telomerase inhibitor treatments undergoing FDA Phase I trials for the treatment of solid tumors, non-small cell lung cancer, breast cancer, multiple myeloma and chronic Lymphoproliferative disease in humans. Initial results have shown an inhibition of telomerase and is helping the company determine optimum dosing for the ongoing trials. The company is conducting FDA Phase II trials on a telomerase cancer vaccine (designed to teach the immune system to recognize and fight cancer cells) for acute myelogenous leukemia. Thus far, the company has reported that these trials are demonstrating a strong safety profile and robust immune responses.

The successful advancement and FDA approval of any one of these treatments would be as valuable as an FDA-approved stem cell spinal cord injury therapy. Thus, the potential valuation of GERN could be up to 10 times that considered when examining the potential value of the spinal cord therapy alone.

And the Geron story does not end with these treatments, as the company also holds an exclusive license to the nuclear transfer technology patents that allow animal cloning, and owns Roslin Bio Med, the commercial subsidiary of the company that cloned Dolly the sheep, the world’s first cloned animal. Under a joint venture with Exeter Life Sciences, Inc., GERN in 2008 formed ViaGen, Inc., which will manage and license the broad portfolio of animal reproductive technology intellectual property rights. Among the commercial applications expected to be offered are cloning for desired genetic traits, such as disease resistance, improved meat quality or yield, an increased milk production. This commercial application may come into play sooner than many think, as the FDA ruled in 2008 that meat and milk products from cloned animals are safe to eat. As this is such a relatively new field, not to mention controversial, the author will not attempt any stab in the dark valuation estimates.

GERN has telomerase licensing deals with Merck & Co. (MRK), and with Sienna Cancer Diagnostics. The company has no debt and enough cash in the bank to run its trials and research for the next two years, by which point it should be earning some revenues from ViaGen and from its licensees.

Without any FDA approvals placing a value on its products, and thus the potential value of its stock, it's truly like throwing knives in the dark, but the potential value is so astronomical that this stock must have the best risk-reward ratio in the field of biotech.

Disclosure: Long GERN

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  •  
    As a long time Geron shareholder, I agree with this assessment of the incredible potential of this company. However, I believe the statement that the current stem cell trial will enroll patients with "essentially a severance of the spinal cord resulting in complete loss of motor and sensory function below the break" is incorrect. The injury that they will be treating in this first trial is a crushing, or contusion, of the spinal cord, not a severance. You can hear the CEO making this specific distinction on the recording from the recent Needham conference.
    Jun 12 11:45 AM | Link | Reply
  •  
    Biotrader's comment on the treatability of crushing type of spinal chord injury is correct.
    The number of 50,000 serious spinal chord injuries per year needs to be reconsidered. My recollection is Tom Okarma had mentioned a number closer to 11,000.
    I'm a very long term long on Geron and I continue to be long because they are making good but slow progress in so many areas, requiring only one to work to be a large financial success.
    Jun 12 01:14 PM | Link | Reply
  •  
    Good article. It's hard to believe anyone would be apposed to these medical breakthroughs. I wonder if those apposed would change their minds if they, or someone they love, suddenly couldn't walk anymore. I am confident Geron will succeed. Years from now people will look at stem cell therapy like a blood transfusion or an organ transplant. You can not undiscover something.
    Jun 12 03:07 PM | Link | Reply
  •  
    Kudos for stating the facts on the wonderful drugs in the pipeline and their enormous potential. However, obviously Mr. Moye under-estimates the value placed on recovering from such a devestating injury/condition. The only thing close to this type of miraculous event would be a cure for cancer! I sincerely believe that anything that could restore even limited mobility to a paralyzed individual would be worth many times more than the $100,000 price tag stated for fixing a broken heart. But, not to be to overly optimistic, lets just go with a 2X figure and then using Mr. Moye's math, we arrive at $200 a share.
    Jun 13 11:43 PM | Link | Reply
  •  
    Thank you all for your comments, and pointing out where I may have erred. I'm going to ask Seeking Alpha to correct a mistake–it is not the 50,000 or so "Americans" who suffer devastating spinal cord injuries every year. It is the roughly 50,000 to 60,000 people worldwide (11,000 to 12,000 Americans). Am also looking into the "crushing" versus "severance."
    JM

    [This correction has now been made - SA editors]
    Jun 15 11:50 AM | Link | Reply
  •  
    Everyone here acts as if this is proven science. It is a SIN! Killing babies for experiments is wrong and anyone who thinks this will work is wrong to. Other countries have already done their frankenstein experiments with HESC and the outcome was death, tumors, and cancer. Why will Geron's trials work? Using realistic math, I arrive at $0 per share after it's a complete failure.
    Jun 17 06:09 PM | Link | Reply
  •  
    Dr.Okarma (ceo of Geron) said in an interview with bbc,"We can cure every spinal cord injury in north america from one embryo". I ask you, what is a "SIN"? Using something smaller than a pencil eraser to cure thousands of people with spinal cord injuries, heart disease, cancer,etc.etc.etc. Or letting it go to waste as it surely will for abortion is a safe and legal practice in the U.S. Go on Youtube and type in stemcells and open your eyes. A girl was blind and now she sees, a man was paralyzed from the waiste down and now he walks. They had to travel great distances to get treatment for something that should have been performed here in the U.S. It's not a matter of if it will work, it's a matter of convincing everyone apposed that they aren't going to hell if they get treated. Geron's stock will be in the hundreds or higher next year when the first person starts walking. When the cancer stuff comes out, thousands.


    On Jun 17 06:09 PM Steven Jackson wrote:

    > Everyone here acts as if this is proven science. It is a SIN! Killing
    > babies for experiments is wrong and anyone who thinks this will work
    > is wrong to. Other countries have already done their frankenstein
    > experiments with HESC and the outcome was death, tumors, and cancer.
    > Why will Geron's trials work? Using realistic math, I arrive at $0
    > per share after it's a complete failure.
    Jun 19 10:32 AM | Link | Reply
  •  
    I'll tell you what - thanks to irrational exuberance and greed, if GERN were to announce ANYTHING positive - as in a toe wiggling - such speculation would occur as to cause the stock to shoot to 20-30 overnight.
    Jun 21 11:28 AM | Link | Reply
  •  
    After it shoots up and starts to come down,SELL! I'm gonna wait for it to lose 15-20% of it's gain then sell 50%. It won't be profitable til FDA gives the green light and that may take another year or so. Buy it up while it's cheap.
    Jun 22 11:55 AM | Link | Reply
  •  
    Youtube? There's a reliable source. I can find info on stocks and watch teenagers fighting all on the same site. Advanced Cell Technology(ACTC) figured out how to cure degenerative eye diseases that cause blindness using the patient's own skin cells. So there's no need to destroy embryos if skin cells work just as good.


    On Jun 19 10:32 AM Titus Andronicus wrote:

    > Dr.Okarma (ceo of Geron) said in an interview with bbc,"We can cure
    > every spinal cord injury in north america from one embryo". I ask
    > you, what is a "SIN"? Using something smaller than a pencil eraser
    > to cure thousands of people with spinal cord injuries, heart disease,
    > cancer,etc.etc.etc. Or letting it go to waste as it surely will for
    > abortion is a safe and legal practice in the U.S. Go on Youtube and
    > type in stemcells and open your eyes. A girl was blind and now she
    > sees, a man was paralyzed from the waiste down and now he walks.
    > They had to travel great distances to get treatment for something
    > that should have been performed here in the U.S. It's not a matter
    > of if it will work, it's a matter of convincing everyone apposed
    > that they aren't going to hell if they get treated. Geron's stock
    > will be in the hundreds or higher next year when the first person
    > starts walking. When the cancer stuff comes out, thousands.
    Jun 22 03:10 PM | Link | Reply
  •  
    You have all got to be kidding. Big Pharma will buy this company out in the next year or so. As long term investors we will be lucky to get $20-$50 per share. Were the risks worth it?
    Jul 03 08:56 AM | Link | Reply
  •  
    What makes you so sure? With the potential value of the stuff geron is working on, I don't think they would give it up so cheap. Partnership perhaps.


    On Jul 03 08:56 AM jean_kirkpatrick@yahoo... wrote:

    > You have all got to be kidding. Big Pharma will buy this company
    > out in the next year or so. As long term investors we will be lucky
    > to get $20-$50 per share. Were the risks worth it?
    Jul 04 10:29 PM | Link | Reply
  •  
    Jamie - What do you think of the FDA delay that was announced today?
    Aug 18 01:57 PM | Link | Reply
  •  
    Not happy about it, especially given how slowly the FDA moves. Curious about the what this new non-clinical data might be, and wish the company was a bit more forthcoming about it.
    Still believe the company has tremendous potential (most people tend to ignore its oncology efforts) and will buy more, especially if the price drops below $5.
    JM of BAM
    Aug 19 10:53 AM | Link | Reply
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