US Food and Drug Administration finally approved the plan by Dr. Burzynski and his team of cancer drug. This is an unprecedented, because until now only large pharmaceutical companies, possessing a gigantic budget, be able to apply for the introduction of drugs on the market.
“We did it, what no one has done, because everyone looks, to get money from the government or pharmaceutical companies. Sell your soul. I have not sold your soul, I did it, what I thought was right. I believe, that we can save many lives and moving forward, that meanness is attacking us, This is the normal case. The larger attacks, the results have improved” - Said in an interview with “New Dziennik” Dr. Stanislaw Burzynski.
The new drug was approved for the treatment of certain types of liver failure, as well as to combat malignant brain tumors, and a kind of leukemia. Soon will go to pharmacies, thus becomes widely available - this from a doctor, will depend, or prescribe to the patient, or not. To, whether it will be refunded, this will depend on the insurance company.
Polish doctor uses a novel method of cancer treatment, wherein the keywords are the so-called Antineoplaston. Are specific peptides and derivatives of the amino acids present in the urine. Historically, this process has relied on extraction from human urine, Today the drug is prepared by synthesis. According to the doctor, they strengthen the immune system, preventing the development of cancer. In addition, the patient is administered suitably formulated together medicament.
“Cancer is not one disease, there is 1000 different types of cancer. They differ in gene structure, This does not recognize the microscope. The same method will not work for all people, because every therapy has to be chosen individually. That many doctors do not know. But we have special descriptions of our methods, we want to publish it in medical journals. If it succeeds, I think, it will be a revolution in the treatment of cancer. The only question, how quickly doctors begin to apply our method - says Dr. Burzynski and adds, Unfortunately, not all that far, you can save. - Some patients have such genes, for which no medicine does not work. Their treatment requires further research”.
Clinic Dr.. Burzynski's Houston. Each, who would like to get information on treatment options, may call: (800) 714-7181.
http://www.dziennik.com/wiadomosci/artykul/lek-doktora-burzynskiego-wkrotce-w-aptekach
Stanislaw Burzynski - Dr. growing hope
With Dr. B, as they call it sick, talking Andrzej Kazimierczak
In Lublin remember his experiments with human urine at the Medical University. Today in Houston, Texas, Dr. Stanislaw Burzynski clinic leads, which is developing a novel method of treatment for cancer patients. After years of battle in the courts and allegations of fraud can take patients back. About his struggle for hope for the sick says "Dziennik Land".
Andrzej Kazimierczak: It is said of the Lord as "Doctor of Hope". Is this hope even more increased after the recent decision of the agency's Food and Drug Administration (FDA)?
Stanislaw Burzynski: - No doubt it. This ruling is the change in the FDA's decision two years ago, when ordered us to halt the admission of new patients for treatment antyneoplastonami. Although this did not stop our business, he completed the second phase of the program these drugs, However, it would not allow to save many people with advanced cancer. Some, unknown number of people just died, but this fact - as you know - the bureaucrats do not matter.
That decision was not, happily, for clinic irreversible effects?
- W 2012 the FDA largely blocked the activity of our clinic, prohibiting the admission of new patients. It happened after this, died as a 6-year-old patient suffering from a brain tumor. This decision was the more controversial, that the percentage of children suffering cured from this disease in our clinic is 20 percent. Let us remember, that is the highest average in the country. A year ago, while the same government agency issued a warning, that "expresses concern about the safety of the patients'. Now suddenly changed her mind.
With the new ruling, we can finally move forward with research. FDA lifted because a limit on research in my clinic in Houston and we can practically resume. This is the third phase, which is the last step before the official approval of the drug. In addition, we take on the treatment of these patients, who do not have a chance to clinical trials. Such studies are in fact limited to certain diagnoses and not all patients may be admitted. FDA therefore concluded, that I can help people, who previously had virtually no help.
Currently, much larger than ever number of people can hope for a cure thanks to your drugs?
- Absolutely yes. To give some perspective here remind, that the disease incidence of brain tumors, where we specialize in the treatment of, in the United States is about. 100 thousands. Most of these patients die, because the treatment is ineffective, with the exception of those few cases, which can be operated in an early stage. If we can cure about with us. 20 proc. patients with glioblastoma, a cure rate for other tumors is even higher, This can be calculated, that we are able to save a large number of people. How much? Well let's say, that the inhabitants of a medium-sized city. On the other hand, there are only theoretical considerations, because, in fact, such a large number of patients are not able to cure. If, however, our drugs are approved for general use, that this could happen in practice.
What is the difference between the second and third phase of testing each drug?
- Approval of the drug in the US is based on the so-called. three phases of clinical trials. In the second phase you have to prove, that the drug is effective in a number of patients. In the case of a brain tumor was show, that due to tumor therapy is reduced or even completely disappears. We conducted such research 14, proving, the disappearance of the tumor was observed in such patients percent, What is required. But that's not all. These tests ran for a long period, so we can demonstrate, that these people live very long - 15 or 20 years. On this basis the FDA granted the status of "breakthrough designation", that is, a breakthrough treatment, when you need to demonstrate a high survival rate of patients. These breakthrough treatments, and is currently used for many drugs in the United States. We will strive for the status of our medicines, because we have a clear reason for doing so. At the same time, we will conduct an intensive study of the third phase, to more accurately determine the, how drugs work.
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The therapeutic activity of Dr.. Stanislaw Burzynski began, when, as a student of the Medical University in Lublin found, the blood of cancer patients are not three compounds present in healthy, which gave rise to the discovery antyneoplastonów. This was in 1966 r. Dreams of the practical application of the discovery directed him to Houston, Texas. There in 1977 r. founded the clinic. The 1984 r. Texas Board of Medical Examiners sued him first process. Then came the federal service. The 1997 r. Dr. Burzynski was acquitted him after a lawsuit by the FDA. He was threatened with the multi-million dollar fine and 290 years in prison. The 2012 r. FDA blocked the activity of the clinic, Dr.. Burzynski. In July this year. This decision was canceled.
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How long will the third phase?
- The third phase usually lasts a long time - from five to seven years. It costs a lot of money. Currently estimated to, that will be needed for this purpose over 40 million. It seems to me, however,, the third phase will be able to run in parallel with the research needed to achieve a "breakthrough designation", and shorten its duration.
Can we accept, that the FDA's decision to the Lord and the clinic of Dr.. Burzynski no longer threaten lawsuits?
- I certainly do not threaten us with the FDA, but we must not forget, we still have dangerous strikers against each other. Let us remember, For the last two years took total war, the aim of which was once again full liquidation of our business. The war began in the typical Soviet-style, when we are persecuted, first in a small, the local newspaper, and then there was slandering columns largest newspaper in the United States. These people are paid from certain sources hostile to us and still have money for their activities. It is still under attack by state organizations, but to a favorable decision probably soon cease FDA. Especially, that the major players in the campaign directed against us slowly withdraw from its activities. The others just lonely cowboys, who still want to shoot, but do not really know, where is the aim of ...
The current situation reminds me of some western script, where the rich rancher wants to get rid of bad cowboys. Hires the right man, in the film can be a John Wayne, that the trick to the very end. In our case,, the hearing will take place soon. I believe, that there will be an investigative journalist, that will show how hostile the environment we are corrupt and as such, sooner or later, will have to disappear. Conducted a campaign against us, not only in the US, but also in Poland, England and even in China, but the main adventurers slowly begin to withdraw from this unproductive activity. Inferior players are still trying to do something, but they have no chance, as evidenced by the recent decision by the FDA.
Is the start of the third phase may be, that patients will have a chance to free treatment?
- We will accept for treatment of patients from around the world, providing them with free drugs. But we must remember, that taking on treatment is selective and not all patients may be subjected to our therapy. However, if you have already been accepted, get it for free drugs, while laboratory tests remain payable whether medical or nursing staff.
They can also expect to undergo treatment outside of Texas?
- Naturally, so, but only when, the rise of our subsidiaries outside the United States. We are going to introduce our therapies in multiple clinical centers in the world, which will be conducted by the best specialists in this field, but this is only the plans for the future. In the meantime, we hope, that we will be definitely approved drugs and doctors will be able to be widely used. It should be stressed, that so far no cure for a brain tumor has not passed the third phase. All were approved after the completion of the second phase and are available on the market. We went a step further.
Is the choice of treatment depends on the cancer patient, for example, by race?
- We use personal approach, assuming, that every patient is different. We have patients from all over the world, but in choosing the method in any case we do not take into account the country of origin. We study the genes and on the basis of tests to make gene therapy patients. The obvious is the question, that e.g.. patients in China is different gene composition than those from Europe and Africa. It is also known, that the people of the so-called. Third World better give up our treatment, because they have a better attitude to modern medicine. As there are so many varieties of cancer treatment is always individualized and each patient requires a separate approach.
Are you educating their successors, who will continue to fight against such a formidable opponent for humanity which is a tumor?
- In our clinic, we have a number of doctoral students, who are currently learning about our treatments will be able to run this business for the benefit of future generations. In addition, oncologists come to us from different places in the world, to take a closer look at our methods. For example,, center based on our experience began in Japan. And tomorrow (8 July. - Editor. red.) I expect the visit of a delegation from Thailand with a high probability can post, the doctors in this country will follow in the footsteps of the Japanese. In the near future we will open our center in Spain and probably in several other countries.
And when in Poland?
- In Poland, unfortunately, not, because the medical community on the Vistula are inimical to us, but just have a lot of luck in human medicine, Polish who come. In the past, lined up his hand for cooperation, but repeatedly met with denial, So probably a great progress in this area should not count.
Thank you for the interview. I wish you continued success, and the patients recovery.
Stanislaw Burzynski - Dr. growing hope
