Consumers Against High Drug Prices
Exposing The FDA's Regulatory Quagmire
CoQ10 Wars
Assembly Line Medicine
Collapsing Within Itself
Intolerable Delays!
"Unsustainable" Cancer Drug Prices
How Government Treated Those For Whom We Now Celebrate Holidays
Horrific Conditions Inside Drug Factories
When "Rules" Are Broken
Federal Death Panels
Science by Ambush
The Looming Doctor Shortage
Former FDA Commissioner Admits Risk of Bureaucratic Delay
FDA Says Walnuts Are Illegal Drugs
The FDA's Most Heinous Drug Approval
No Real Healthcare Cost Crisis
FDA Delay of One Drug Causes 82,000 Lost Life-Years
Deadly FDA Neglect
How Much More FDA Abuse Can Americans Tolerate?
Drug Company Pleads Guilty to Health Fraud
Why American Healthcare is Headed for Collapse
The Generic Drug Rip-off
Ending the Atrocities
Millions of Needless Deaths
Would You Tolerate This Abuse?
The FDA Indicts Itself
The FDA's Cruel Hoax
Fish Oil Now Available by Prescription!
FDA Threatens to Raid Cherry Orchards
Inside the FDA's Brain
FDA Fails to Protect Domestic Drug Supply
FDA Permits New Fish Oil Health Claim
FDA Approves Deadly Drugs, Delays Lifesaving Therapies
The $50.00 Toll Bridge
Dangerous Medicine
Cardiologists Overlook Lifesaving Discovery
What You Don’t Know About Blood Sugar
Jerry Falwell Attacks Life Extension Foundation
Life Extension Achieves "Impossible" Victory in the U.S. House of Representatives
Fighting the FDA
Patient Advocates Sue FDA Over Drug Access
FDA's Lethal Impediment
Don't Blame the Doctors
One Man's Ten-Year Ordeal With Prostate Cancer
A New Day At FDA?
The FDA Versus the American Consumer
Supreme Court Roundup
The Lethal Information Gap
Consumer Rape
Dying From Deficiency
Are Offshore Drugs Dangerous?
Drugs the FDA Says You Can't Have
Does Cholesterol Cause Artery Disease?
What's Wrong with the FDA
FDA Suffers Second Massive Legal Defeat in Pearson v. Shalala
FDA Loses Case Against Compounding Pharmacies on First Amendment Grounds
Ending The Cancer Bureaucracy
Victory in the House and Senate
Life Extension Wins in the House and Senate
Congress Recognizes The Prescription Drug Problem
Americans are getting Healthier... But the FDA Remains a Major Impediment
Are We to Become Serfs of the Drug Monopoly?
A Glorious Victory Over FDA Tyranny
The Great American Rip-Off
The Plague Of FDA Regulation
Health Costs to Double Is there a free-market solution?
The FDA versus Folic Acid
They Want You Brain Dead
Life Extension vs. the FDA a Hollow Victory: Why the Agency's Approval of Ribavirin is Inadequate
William Faloon

FDA's Lethal Impediment

The FDA stifles the discovery and availability of life-saving therapies by making the cost of getting them approved prohibitively expensive. The FDA is a major obstacle that prevents scientific findings from being translated into therapies to stave off age-related disease.

Compared to the advancement of other technologies over the past 40 years, medicine has progressed the slowest as far as finding solutions for lethal diseases. Those in the medical establishment may debate this assertion, but the undeniable fact is that for most types of cancer and neurological diseases, there have been few substantive improvements in survival, let alone a cure.


Most of you remember attending funerals in the 1960s to 1970s of those who perished from cancer. If you thought the way I do, you would have been certain that a cure for cancer would have been found by year 2000. In fact, the propaganda being released by the cancer establishment at that time was that doctors were on the verge of eradicating most cancers. (This misguided optimism was primarily based on the premise that chemotherapy was the solution.)

When it comes to therapies designed to slow or reverse aging, the FDA still does not officially recognize aging as a disease process. That means when a company tries to gain approval to market an anti-aging therapy, it first has to overcome the hurdle of educating the FDA that aging is indeed a lethal disease. The new therapy then has to show sufficient efficacy to warrant approval. To date, no one has succeeded in convincing the FDA to approve an anti-aging drug.

In today's world of ever-expanding technological achievement, the fact that medicine remains bogged down in a regulatory quagmire is a disgrace. More than 6,000 Americans die every single day, yet most of these deaths could be prevented if it were not for the strangulation of innovation caused by the FDA, State regulatory agencies, HMOs and apathetic physicians.

In each issue of Life Extension magazine, we seek to uncover therapies that have shown efficacy in well-controlled studies, but have not yet been translated into conventional medical practice. We know our efforts have lengthened the lives of tens of thousands of Life Extension members, yet what we offer is only the tip of the iceberg when one looks at the many life-extending drugs that are denied to human beings in need.

Does Geron have an effective cancer vaccine?

Geron Corporation was originally established to develop anti-aging drugs. Their research, however, led them to discover a potentially effective cancer treatment.

On March 18, 2003, Geron released the results of a study that an experimental cancer vaccine might be effective against all types of cancer. This bold announcement was based on a study published in the journal Cancer Gene Therapy (March 2003).

What the public thinks about the FDA-

Beginning May 8, 2003, Life Extension initiated an Internet poll on a website ( that has about 400,000 new visitors each month. The people visiting this site are not part of any anti-FDA group, nor were they exposed to anti-FDA propaganda. These people were asked a simple question as to whether terminally ill cancer patients should have the right to any drug that might save their life. After 22,506 votes were tabulated, here are the results:

Terminally ill cancer patients
Should have access to any drug that might save their life: 89%
Should only have access to drugs approved by the FDA: 11%

We live in a constitutional republic where the people's wishes are supposed to be adhered to (as long as they don't infringe on the rights of others). If 89% of the American public thinks terminal cancer patients should have access to any drug that could save their life, then there is no reason for the law not to be changed to allow this. Companies that engaged in fraud could be prosecuted under consumer protection laws that already exist. The FDA could post its opinion about the safety and efficacy of purported cancer therapies on their website ( The civil litigation risks to companies that knowingly sold bogus products would preclude large-scale unsavory activities that a minority of Americans fear. The greater fear Americans face is being diagnosed with cancer only to find out that a potential cure is too many years away to save their lives.

Of interest was an identical poll on Life Extension's website ( in which 98% of people voted to allow cancer patients to have access to any drug that might save their life. This is not surprising considering health conscious people's animosity towards the FDA.

Geron's vaccine works in a relatively simple manner. It programs powerful dendritic immune cells to attack cells that express high levels of an enzyme called telomerase. It just so happens that 85% of human tumor cells overly express telomerase1 whereas normal healthy adult cells express very low and/or transient telomerase levels. Using telomerase as the target for dendritic cells, Geron's vaccine was shown to provoke a massive attack against prostate and kidney cancer cells as well as breast, melanoma and bladder cancer.

Most cancer cells require high levels of telomerase to prevent them from undergoing a healthy cellular removal process called apoptosis (programmed cell death). The concept of attacking cells high in telomerase makes cancer cells particularly vulnerable, because if they try to hide from this vaccine by making less telomerase, then they will die via normal apoptosis.

There are 558,000 people in the United States who will die of cancer over the next 12 months. Most of them know they are likely to die. We believe these cancer-stricken individuals should have the right to access any potentially effective therapy under the guidelines of an objective yet humanistic formal scientific protocol. While there is no assurance that Geron's new vaccine will cure cancer, we vehemently oppose the power given to the FDA to withhold this and other potential cancer therapies.

The cancer establishment maintains that only carefully controlled studies can establish safety and efficacy. This sounds reasonable and Life Extension agrees with this concept. The reality, however, is that the FDA's current clinical trial requirement has produced flawed data that enabled bad drugs to be approved while potentially effective drugs are denied.2,3,4

It takes so long for a new drug to make it through the FDA approval process, that if Geron's new drug is effective, most cancer patients reading this column today will perish long before the vaccine ever became available. A real world example of this occurred with an anti-cancer agent for childhood leukemia called Vumon®. This drug was first studied in 1972, but only attained FDA approval in 1992.

A Phase I study of Geron's telomerase vaccine is currently underway in patients with prostate cancer at Duke University in North Carolina. As described in previous issues of Life Extension magazine, there are two fundamental problems with Phase I studies. First of all, they usually mandate that cancer patients fail all "proven" therapies first. As has been repeatedly shown in published scientific studies, most so-called "proven" cancer therapies do not cure the disease. Since Phase I studies only test for safety, extremely small doses of the anti-cancer agent are used. This dooms virtually all the terminal cancer patients who participate in Phase I trials to certain death, but it does supply the FDA with the safety data it mandates. In other words, as long as the patient dies of their cancer and not the new drug, it is now permissible to move on from Phase I to Phase II studies where a potentially effective dose of the anti-cancer drug can be given.

How the FDA perpetuates the cancer epidemic

It is clear that the bureaucratic process is incredibly long for the approval of anti-cancer and other therapies used in the treatment of life-threatening diseases. To add insult to injury, the very same approval process has geographic boundaries that create inhumane and unacceptable delays for approval of a critical drug in one country that may be a few miles away from a country where the drug is already studied, reviewed and accepted.

For example, it took years for Taxotere, one of the most impressive anti-cancer agents used to treat breast and prostate cancer, to finally gain FDA approval in the United States. This occurred despite hundreds of studies supporting its efficacy published in the European literature that were not acceptable to the FDA.

Ironically, now that Taxotere has gained FDA approval for the treatment of metastatic prostate cancer in the USA, countries such as Germany do not permit its use in the treatment of prostate cancer because no published papers on this subject have emanated from Germany. This becomes even more incredulous when one realizes that the pioneering research on Taxotere emanated from Germany's next-door neighbor France. The approval agencies such as the FDA here and its counterparts abroad are allowing bureaucratic ego, and perhaps economics, to interfere with the saving of life. Think about this! American and German physicians and scientists are engaged in a battle against a common enemy (cancer) while the respective regulatory agencies (those that approve the use of a drug) of each country use national borders to say "yes" or "no" to a live-saving drug or therapy. This is a violation of human rights within so-called civilized societies. People from all over the world should unite in protest to such atrocity.

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