Brain Tumor Survivors Visit Burzynski Research Institute, Manufacturer of Life Saving Medication.HOUSTON -- Every year in America, approximately 18,300 people are diagnosed with brain tumors and as many as 13,100 people die from these deadly malignancies. Twelve people who have beaten those odds will gather on Oct. 15, 2004, at the Burzynski Research Institute Inc. (BRI See ISDN. BRI - Basic Rate Interface ) (OTCBB OTCBB See OTC Bulletin Board (OTCBB). :BZYR) in Stafford, Texas, to celebrate their recovery. Beginning at 9:00 a.m., they and their families will tour the facility that manufactures the medication that saved their lives. When surgery is not an option, there is no effective long-term therapy for brain tumors. And, if the diagnosis is a glioblastoma glioblastoma /glio·blas·to·ma/ (gli?o-blas-to´mah) any malignant astrocytoma. glioblastoma multifor´me , the deadliest and fastest-growing brain tumor, the outcome is normally fatal, in a short time. BRI believes there is now increased hope for brain tumor victims. On Sept. 7, 2004, BRI was granted orphan drug orphan drug, drug developed under the U.S. Orphan Drug Act (1983) to treat a disease that affects fewer than 200,000 people in the United States. The orphan drug law offers tax breaks and a seven-year monopoly on drug sales to induce companies to undertake the designation for its drug candidates Antineoplastons A10 and AS2-1 by the U.S. Food and Drug Administration (FDA FDA abbr. Food and Drug Administration FDA, n.pr See Food and Drug Administration. FDA, n.pr the abbreviation for the Food and Drug Administration. ) for the treatment of brain stem gliomas Background: Brainstem gliomas are tumors that occur in the region of the brain referred to as the brain stem, which is the area between the aqueduct of Sylvius and the fourth ventricle. . This designation represents a major milestone in the development of these experimental medications, which have shown promise in FDA-supervised clinical trials at the Burzynski Clinic in Houston. The FDA's orphan drug program encourages research, development and approval of products for diseases that affect fewer than 200,000 patients in the United States each year and that provide a significant therapeutic advantage over existing treatments. The dozen long-term survivors gathering at BRI had aggressive brain cancers. Four of them had glioblastoma multiforme glioblastoma mul·ti·for·me n. A virulent brain cancer that is usually fatal. , the most aggressive form of brain tumor. Those diagnosed with a glioblastoma have a prognosis of less than 1% probability of living 6 months. There are generally no long-term survivors. "These former patients have all survived and are back at work and enjoying normal lives," reports Dr. S Dr. Doctor. dr. dram. .R. Burzynski, founder of BRI and the Burzynski Clinic. "Some of them are celebrating 10+ years of being tumor-free since their cancer diagnosis." Dr. Burzynski, Dr. Robert Waldbillig, BRI's vice president of research, and the survivors will be available for questions and interviews at the completion of the tour. "Bringing this many brain tumor survivors together is truly amazing," says Paul Leverett, managing director of the Burzynski Companies and himself a glioblastoma survivor. "No other cancer treatment center that I know of could do this." At its pharmaceutical manufacturing facility, located at 12707 Trinity Dr. in Stafford, Texas, BRI manufactures the active pharmaceutical ingredients (APIs) for Antineoplastons A10 and AS2-1. It also produces the finished antineoplastons medications, the injection and capsule forms used by the Burzynski Clinic. BRI's Department of Molecular and Cellular Biology cellular biology n. The study of the molecular or chemical interactions of biological phenomena. conducts genetic and biochemical research to understand the mechanisms of action of antineoplastons in cancer cells and develop new and more potent formulations of antineoplastic drugs. Forward-looking statements in this release are made pursuant to the safe harbor Safe Harbor 1. A legal provision to reduce or eliminate liability as long as good faith is demonstrated. 2. A form of shark repellent implemented by a target company acquiring a business that is so poorly regulated that the target itself is less attractive. provisions of the federal securities laws. BRI cautions investors not to place undue reliance on the forward-looking statements contained in this press release. Information contained in forward-looking statements is based on current expectations and is subject to change, and future events may differ materially from those discussed herein due to a number of factors, including, but not limited to, risks and uncertainties related to BRI's ability to obtain regulatory approval for Antineoplastons A10 and AS2-1. Receiving orphan drug designation does not increase the likelihood of eventual regulatory approval for a product candidate. BRI does not undertake to update any such forward-looking statements or to publicly announce developments or events relating to the matters described herein. |
|
||||||||||||||

Printer friendly
Cite/link
Email
Feedback
Reader Opinion