Neuralstem in the News

 

  • Richard Garr interviewed on NPR Kojo Namdi Show

NPR Kojo Namdi Show

WASHINGTON The FDA is giving a thumbs-up to the first human trial involving embryonic stem cells. The study, which will examine the safety of this treatment in people with spinal cord injuries, comes in advance of a widely-anticipated shift in U.S. policy on embryonic stem cells. Join Kojo as we explore the intersection of bioethics and stem cell research

Listen to the program at the WAMU website or download the podcast from NPR's website

  • Stem cell interests buoyed by Obama promise

Gazette.Net

A sea change in stem cell industry investment is coming, says Richard Garr. The CEO of Gaithersburg-based Neuralstem happened to be in New York last week, pitching his company to prospective investors, when a member of President-elect Barack Obama's transition team said one of Obama's first priorities as president will be to lift the federal ban on funding embryonic stem cell research imposed by President Bush nearly eight years ago.

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When he returned to his biotech this week, Garr said, he had found that "the general feeling in the investment community is that this is going to be a stem cell-friendly administration and a stem cell-friendly Congress." Even in today's difficult investment climate, the stem cell industry is going to see definite benefits, he said.

Human stem cells can be grown into healthy sources of new cells, tissues and organs to help scientists find treatments for diseases such as Alzheimer's, Parkinson's, diabetes and cancer. Some oppose embryonic stem cell research because they believe extracting cells from a viable embryo destroys a human life.

Investors mostly look for signs of progress, politics aside. Garr said he felt "warm interest by investors" at the Acumen BioFin Rodman & Renshaw ninth annual Healthcare Conference in New York because Neuralstem is ready to file an investigative new drug application for the first time and will enter clinical trials with a stem cell drug for amyotrophic lateral sclerosis, or Lou Gehrig's disease, this winter.

"The timing [of the Obama statement] is very good for us," he said.

A change in the federal policy won't directly affect Neuralstem, he said, because his company doesn't receive federal or state money.

But, he said, "It will be a good thing if [Obama] lifts [the funding ban] because it will change the public perception of stem cell companies. … It will remove the uncertainty of whether or not this is going to be a legal industry. That is huge."

Douglas Doerfler, president and CEO of MaxCyte in Gaithersburg, who testified at a U.S. Senate hearing on the issue in 2005, agreed.

"I believe it will be a huge boon for companies who have been involved in stem cells [and] several are located in Maryland," Doerfler said. "This is a phenomenal area of science, and watching this field closely adds a sense of marvel at the progress being made, especially in regenerative medicine."

Doerfler cautioned, however, that lifting the ban comes late for the U.S. to get "back in the game," as other nations have invested heavily in the promise of stem cells and took competitive advantage while the U.S. was not playing a major role.

Linda Powers, managing director and co-founder of Toucan Capital in Bethesda, Maryland's most active stem cell investment firm, said lifting the ban would be "just the first step" in making the industry more fluid. She hopes, for example, that treatments for heart disease, multiple sclerosis and other serious conditions now being developed in other countries using patients' own bone marrow cells would be developed here without the current requirements of years of clinical trials.

Other restrictions, she said, include regulatory "artificial efficacy" rules on stem cells.

"They are held to much more difficult standards than other medical products," said Powers, a member of the Maryland Stem Cell Research Commission.

Even if the stem cells used are a patient's own, eight to 10 years of clinical trials and hundreds of millions of dollars of expenses are required. "If a patient's own stem cells are used in a therapy, they are regulated as a drug just as stem cells that are not from the patient's own body," Powers said. "That is just plain crazy."

Commercial stem cell research operates in "a very restrictive patient environment as well," which could loosen if federal policies are changed, said Jonathan Auerbach, CEO of GlobalStem, Inc. of Rockville.

Funded partly by Toucan, GlobalStem sells bio-tools for stem cell researchers, such as growth media to feeder cells, characterization tests and assays. Lifting restrictions, Auerbach said, would help because some of the limited embryonic cell lines that are available, called the Bush lines, are old and are "not the best cell lines."

Bowen P. Weisheit Jr., a member of the state stem cell commission and of the state chapter of the Cystic Fibrosis Foundation, said that if Obama lifts the ban, he thinks the effect on current proposals would expand.

This report originally appeared in The Business Gazette.

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  • Neuralstem CEO, Richard Garr, featured in CNNmoney.com

CNNMoney, April 09, 2008

NEW YORK (CNNMoney.com) -- The Food and Drug Administration looks like it's bowing to the inevitable this week and drawing the blueprint for the first-ever human experiments with human embryonic stem cells.

FDA advisors meet Thursday and Friday to begin to design how these embryonic stem cell tests will be conducted. It's an important regulatory step that could lead to human testing as early as this year. So far, biotechs have tested their spinal-cord drugs in animals, not people.

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"[The FDA meeting] is the first step towards clinical trials," said Laurie Zoloth, professor of medical humanities and bioethics at Northwestern University. "It's an important moment. And it's only the very beginning."

Human embryos are prized by medical researchers because of their fast and malleable regenerative properties. In theory, they could be used to heal severed spines, as well as damaged or diseased brains, hearts and other organs.

But their use is one of the most controversial issues in medical research, a controversy that centers on whether embryonic cell groupings, called blastocysts, are considered human life.

Dave Prentice, senior fellow for life sciences at the Christian organization Family Research Council, opposes the use of human embryos in research. "You shouldn't be destroying human embryos at the earlier stage of human life to harvest cells," said Prentice, who has a PhD. in biochemistry from the University of Kansas.

Other stem cell options are available, he said, such as harvesting them from umbilical cord blood or adult tissue, or "reprogramming" adult cells to behave like stem cells, as demonstrated in recently-released but early-stage studies.

Zoloth said she supports stem cell research because "the human embryo does not have the moral status of a dying child." Like other supporters, she pointed to the vast potential - though still unproven - of this science in healing traumatic injuries and degenerative diseases.

"I strongly support learning as much as we possibly can about human embryonic stem cells, as well as learning about other types of regenerative medicines," she said. "The fact that science could develop ways of healing very tragic human fates is an extraordinary capacity that we have been given by God. For people who aren't religious, you might say that we stand in a remarkable moment in human history."

Safety over ethics for the FDA

The FDA seems to be more concerned with the stem cells' possible side effect of producing tumors. Because of the "potential risks" of human embryonic stem cell products, data showing a drug's effectiveness "may need to be particularly strong," the document said.

An administration spokesman would not comment further than the released document.

"The FDA needs to feel comfortable that the cells we use for our cell products will not cause teratomas," said Alan Lewis, chief executive of privately-held biotech Novocell, which hopes to begin human stem cell testing within three years for a possible diabetes treatment.

Lewis described the teratomas as non-malignant but unwanted pieces of muscle, hair or other matter that form as an offshoot of embryonic stem cells, which replicate quickly and can morph into different types of tissues, such as the liver or pancreas.

The biotechs line up

Geron (GERN) could be the first company to conduct experiments in humans with drugs made from human embryonic stem cells. The biotech is developing a treatment to repair spinal cord injuries. Geron has already filed an application to the FDA to begin human testing, according to analysts. But the biotech refused to confirm this and would not discuss the upcoming meeting.

So far, Geron's animal experiments have been tumor-free, said UBS analyst Graig Suvannavejh, who doesn't expect the company to run into problems with the FDA.

"For Geron, the best possible outcome overall is for [the] FDA to be peachy with everything they've done so far," said Suvannavejh in an email to CNNMoney.com. He believes Geron could begin human testing by mid-2008.

Steve Brozak, analyst for WBB Securities, emphasized that tumor-safety is imperative, and there is little room for failure in the current environment.

"It is one of the things that can be a problem if the science is not understood completely," he said. Geron needs "to make sure that the critics of the field don't have room to assail them with."

Advanced Cell Technology is using embryonic stem cells to develop a treatment for vision loss. Chief scientific officer Robert Lanza said his company plans to file an application for human testing to the FDA within months. He said the company has found a way to "differentiate" stem cells to reduce the possibility of tumor formation.

Neuralstem (CUR) works with stem cells derived from a donated human fetus, rather than embryonic stem cells. CEO Richard Garr said his company is developing a treatment for Lou Gehrig's disease, which degrades spinal cord nerve cells. He intends to file an application for human testing to the FDA in September or October.

Garr said that his company's pig tests have been tumor-free, and he hopes the FDA panelists focus on the science of stem cells, not the controversy, in designing requirements for clinical trials.

"What we hope to come out of this meeting is rationality," said Garr. "[We] hope that this isn't just something that a stem cell-unfriendly administration is trying put in place before they leave."

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  • Microsoft Money contributing writer Michael Brush recommends Neuralstem for model portfolio

MSN Money by Michael Brush

If holiday shopping has blown your budget, here's some relief: Wall Street is offering bargains.

The stocks of many small yet promising companies have been hammered as nervous investors have shifted funds to the perceived safety of big businesses with proven track records.

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Here's the upshot: There's a fresh crop of stocks under $5 a share that could double in a year as investors come to their senses and realize the subprime-mortgage debacle won't bring economic Armageddon.

My five favorite stocks selling for less than the price of a Big Mac meal are stem-cell-research company Neuralstem (CUR, news, msgs), flat-panel-TV designer Syntax-Brillian (BRLC, news, msgs) and energy companies Teton Energy (TEC, news, msgs), International Royalty (ROY, news, msgs) and Abraxas Petroleum (ABP, news, msgs).

These stocks may see a bounce soon because of the January effect -- a rebound once the pressure of year-end tax-loss selling abates. But the bigger gains will come after some key changes in investor psychology play out.

"This is a flight-to-quality market, so anything perceived as risky has had a really hard time making headway," observes Eric Barden, a co-portfolio manager of the Texas Capital Value and Growth Fund. "But when this turns, it is going to turn really fast."

When is the turnaround coming?

Barden thinks it could be six months before investors develop an appetite for riskier small-cap stocks.

But I think he may be in for a surprise, and our under-$5 stocks could bounce back sooner than that. Here are four reasons why, thanks to James Paulsen, an economist and market strategist with Wells Capital Management:

  • We've been waiting at least six months for the subprime disaster and housing weakness to bring down the economy. So far, they haven't. Employment and wage growth are hanging in there. Consumer spending was solid in November. Foreign demand for the goods we make is healthy. At some point, investors will realize the much-feared economic disaster ain't gonna happen -- and they'll develop a taste for riskier areas of the markets again, such as stocks selling for less than $5. The underlying conditions are still in place for decent economic growth: falling interest rates, government deficit spending, a weaker dollar and a continued expansion in the money supply.

  • Fears about shortages of liquidity -- the availability of money -- are overblown. Just look at the record levels of personal net worth in this country, the solid corporate balance sheets, currency reserves held by central banks and the amount of investment cash in the sovereign funds of foreign governments. "It's a preponderance of fear that is keeping liquidity in the closet, not a shortage of liquidity," Paulsen says. "If someone says things are OK, then watch the liquidity come out." Wait for signs that subprime-related write-offs are easing or for signs of continued economic strength to calm jitters. Again, a change in psychology will benefit the least liquid stocks the most, including our under-$5 stocks.

  • The weaker dollar helps small-cap stocks as much as big companies, if not more, because the cheap dollar attracts foreign buyers to our shores. Large-cap companies already have an overseas presence.

  • Historically, small-cap stocks do well when there is inflation, which is making a comeback.

So now, here's a closer look at five stocks trading for less than $5 that should benefit from these trends, as well as company-specific developments. To find these stocks, I looked for companies where insiders are buying the most, and I consulted with investors with good records who specialize in this part of the market.

Hope for paraplegics?

Researchers working with the tiny biotech company Neuralstem have discovered that if you implant the right human stem cells into the spines of paralyzed rats, the cells take over and regenerate in a way that allow the rats to walk again. This stunning breakthrough shows the promise of a controversial area of medicine known as stem-cell research.

But would this work in humans? The world is about to find out. By March, Neuralstem may begin testing the same science on humans in a study at the University of Pennsylvania. As early as three to six months later, it could start to see results. If this process, known as regenerative medicine, or cell therapy, shows promise in the study, I'd expect nice gains in this under-followed stock, which recently traded for $2.85 a share.

The Pennsylvania study will test the use of stem cells to treat a kind of paralysis called ischemic paraplegia. This occurs when people have a hemorrhage in the spine, typically because doctors had to clamp the aorta, the main artery from the heart, when treating another problem. Strictly speaking, this is just a "feasibility and safety" study.

"But these will be real patients getting the real thing from the beginning, so we expect to see if we have impact," says Neuralstem Chief Executive Richard Garr.

Later next year, Neuralstem will likely begin testing cell therapy on patients with Lou Gehrig's disease or traumatic spinal cord injuries. The technique might also be used to treat other central-nervous-system disorders, such as Parkinson's and Alzheimer's diseases, and even depression.

Neuralstem is a player in this space because it owns technology that allows doctors to reproduce huge amounts of stem cells and to shut off the reproduction process when enough have been made.

Flat-panel play

If you've been shopping for a flat-panel TV this holiday season, chances are your eyes have gazed on the Olevia brand of Syntax-Brillian, a tiny company based in Arizona that outsources manufacturing to Asia.

In the past four months the company has offered shareholders as much unwelcome drama as the flesh-eating zombies tormenting Will Smith in a futuristic Manhattan in the movie "I Am Legend."

Syntax-Brillian stock has tumbled 60% since early September to recently trade at $2.45 a share. But insiders clearly think investors are overreacting to a couple of pieces of bad news. In the past month, they've snapped up $2.2 million worth of stock.

Syntax-Brillian designs and sells high-definition televisions that use liquid-crystal-display (LCD) technology. It also owns camera maker Vivitar, which it bought in November 2006.

In September, Syntax-Brillian stock got hammered when it said the credit crunch was squeezing Asian suppliers and hurting production. Then it announced a move to a royalty model for sales in China, meaning it would take a small cut of sales by licensing its brand instead of managing production itself. There was also a management shakeup that saw the finance chief exit -- rarely a reassuring event.

Investors are understandably unhappy with all of this, but consumers love Syntax-Brillian's flat-panel TVs, and that's what counts for me. Sales were up 54% in the third quarter. The company is in the sweet spot, selling midrange LCD TVs going for $1,000 or more.

"That is where the demand is right now, and these guys are really well-positioned there," says Mark Mowrey, a tech stock analyst who writes the TechValue Report. He thinks the stock will eventually trade up to $7 a share.

3 natural-resource plays

I believe energy and natural resources will continue to be hot sectors, so I'm including three plays from these areas in my under-$5 picks. The first is Teton Energy, a really small (market cap: $74 million) producer of natural gas in the Rockies. Because pipeline constraints make it hard to transport natural gas out of the Rockies, natural gas is cheaper there. This has hurt producers in the Rockies, but that may begin to change starting next year, Teton chief Karl Arleth explains.

The reason: Kinder Morgan Energy Partners (KMP, news, msgs) and ConocoPhillips (COP, news, msgs) are putting in a pipeline that should increase "export" capacity out of the region by 29% over the next two years.

Meanwhile, Teton should double production capacity next year, and it has enough financial strength to do that without issuing new stock, Arleth says. All of this may explain why insiders have purchased $691,000 worth of stock in the past month, according to InsiderScore.com.

International Royalty generates income by purchasing the rights to future royalty payments from mines producing metals such as copper, nickel and gold. It buys the royalty streams from mining companies that need to generate cash or from owners of mineral rights looking to cash out.

"The company is mainly tied to copper and nickel prices, which have gotten hammered in past three months," says Joe Dancy of LSGI Advisors, an investment company. So International Royalty shares have suffered, trading below $5 recently from above $7 in October.

But Dancy thinks copper and nickel prices will improve because of continuing strong demand from China, India and other emerging economies. He agrees that gold prices should go up because of a weakening dollar. So he thinks International Royalty is a buy below $5.

He's worth listening to because his LSGI Advisors has produced annualized returns of 23.7% a year over the past eight years by investing in small-cap stocks.

In early November, Abraxas Petroleum announced production and sales declines for the third quarter, and its stock has fallen 26% to $3.40. But the company says it can get back into growth mode through exploration and more-efficient production at its properties in Texas and Wyoming. It's also buying properties through a subsidiary called Abraxas Energy Partners, which the company hopes to spin out at some point. Insiders are putting their own money behind the plan. They've purchased $1.5 million worth of stock in the past six months, at prices below $4, a convincing vote of confidence.

Some words of caution

As microcap companies with narrow business plans, these five plays under $5 carry greater-than-average risk that something big could go wrong and derail the stocks. The stocks also have limited liquidity, or average daily volume, which means volatility; bad news could have a big downside.

The limited liquidity can also hurt you in another way: If any of these stocks are up more than 10% because of buying interest generated by this column, I strongly advise you to wait a few days and buy when the interest cools off, so you don't end up paying too much.

I like the prospects for all of these, and I believe overly negative sentiment toward small-cap stocks will reverse, so I'm putting all five of these in my model stock portfolio in MSN Money's Expert Picks section.

At the time of publication, Michael Brush owned shares of Neuralstem.

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  • Rubicon Global Research Buy-Side Investment Analysis

October 9, 2007

Investment Thesis/ Summary Conclusion:

Neuralstem, Inc. is a biopharmaceutical company with a robust and diverse development pipeline derived from its novel and patent protected human neural stem cell (hNSC) technology. The Company's research and development efforts target the treatment of debilitating central nervous system (CNS) disorders for which no effective treatments exists.

 

Select media coverage in this website is provided for the information and convenience of the public, and is not intended to be all-encompassing nor an endorsement of the specific stories or media outlets.

Privacy and Terms ©Neuralstem, Inc. 2014

Crain’s Detroit Business explores NSI-566 next steps with ALS P.I., Dr. Eva Feldman, and reviews additional indication, Alzheimer’s disease, following promising animal research. | 8.1.14
The Wall Street Journal interviews President/CEO, Richard Garr, on patient-directed social media’s impact on trials. NSI-566/ALS patients have independently chosen to blog online. | 7.30.14
FORBES' feature quotes President/CEO Richard Garr extensively, on the differentiation and commercialization of Neuralstem’s proprietary cell technology. | November 2013
FOX Medical Team's Beth Galvin continues her NSI-566/ALS coverage at Emory with a patient’s perspective segment. Phase I patients, Ted Harada and John Conley, are featured. | 11.20.13
Bethesda Magazine feature provides rich insights on Neuralstem’s “potential wonder drug aimed specifically at rebuilding the hippocampus”: NSI-189. | November-December 2013
Practical Neurology interviews Chairman and CSO Dr. Karl Johe and P.I. Dr. Eva Feldman about the NSI-566/ALS trials in “Decreasing Progression, Increasing Function.” | October 2013
FOX News Detroit walks with NSI-566/ALS Phase I patient Ted Harada and P.I. Dr. Eva Feldman on the eve of the Phase II trial. | 8.28.13
Bioscience Technology ALS P.I. Dr. Eva Feldman and Neuralstem’s President/CEO Richard Garr in a feature that explores data from six extraordinary ALS responders – “as rare as a red wolf.” | 5.30.13
MIT's Technology Review reports on CELL SCI research showing “paralyzed rats walk again after stem cell transplant” of NSI-566, suggesting hope for treatment of spinal cord injury. | 9.13.12