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Watson Pharmaceuticals Receives A Complete Response Letter For Its 24-Week Formulation Of TRELSTAR(R) (triptorelin Pamoate) NDA From US FDA
Watson Pharmaceuticals, Inc. (NYSE: WPI), a leading specialty pharmaceutical company, announced that it received a Complete Response Letter from the U.S. Food and Drug Administration (FDA) on its New Drug Application (NDA) for TRELSTAR(R) 22.5 mg (triptorelin pamoate for injectable suspension), a 24-week formulation of TRELSTAR(R) for the palliative treatment of advanced prostate cancer. The TRELSTAR(R) NDA was prepared in cooperation with Debiopharm Group, a Swiss-based global biopharmaceutical group of companies.
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Applied Infectious Disease Epidemiology Conference, Stockholm, Stockholm, October 26-28, 2009
"Epidemiology is always important and topical, though sometimes unsung," says Professor Johan Giesecke, Chief Scientist at ECDC, the European Centre for Disease Prevention and Control, "but the third applied Infectious Disease Epidemiology Conference in Stockholm in October this year will be an opportunity to put Epidemiology and infectious disease prevention and control into the spotlight; delegates will have the opportunity to discuss and share information on current and emerging infectious diseases, including influenza A (H1N1)v. The call for abstracts closes on July 3rd so there is no time to lose."
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UK Autism: MPs Impressed With UK Autism Foundation's Achievements
The member of parliament for Feltham and Heston Alan Keen MP together with his wife, Health Minister Ann Keen MP,(Brentford & Isleworth) wrote to the UK Autism Foundation wishing the "Scope for Hope" autism charity dinner in Feltham every success. Hundreds attended the glittering event, held at the Royal Naval Association Club in Feltham, Middlesex on Saturday 13th June.
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Clinical Trial At The Cancer Institute Of New Jersey Focuses On New Treatment Combination For Most Common Type Of Non-Invasive Breast Cancer

Researchers at The Cancer Institute of New Jersey (CINJ) have launched a clinical trial that targets a new treatment combination for the most common type of non-invasive breast cancer known as ductal carcinoma in situ (DCIS). CINJ is a Center of Excellence of UMDNJ-Robert Wood Johnson Medical School. In DCIS, the cancer cells are inside the milk ducts of the breast but have not spread to surrounding breast tissue. According to the American Cancer Society, one in five new breast cancer cases in the United States is diagnosed as DCIS, and nearly all diagnosed at this early stage can be cured. The trial, sponsored by the National Surgical Adjuvant Breast and Bowel Project (NSABP), will compare the effects of adding the drug trastuzumab to radiation therapy following breast sparing surgery (lumpectomy) in patients whose DCIS makes too much of the protein known as HER2 (positive). Too much of this protein can cause a normal cell to turn cancerous and make existing cancer cells grow faster. Trastuzumab is considered a targeted therapy against HER2-positive breast cancer. Early information shows the drug may also help radiation therapy work better in treating HER2-positive breast cancer, although investigators caution more research is needed in this area. Trastuzumab has approval from the U.S. Food and Drug Administration (FDA) for the treatment of HER2-positive breast cancer together with chemotherapy, but it is considered "investigational" in this trial, because its use in combination with radiation therapy has not been FDA approved. The primary aim of this study is to see if this new combination is more effective in preventing occurrence of DCIS in the same breast or in other parts of the body, versus giving radiation by itself following lumpectomy. Antoinette R. Tan, MD, a medical oncologist at CINJ and assistant professor of medicine at UMDNJ-Robert Wood Johnson Medical School, is the lead investigator of the study at CINJ. "A previous study by the NSABP shows an overall recurrence rate of eight percent in this population 12 years following breast conserving surgery and radiation. If we can add another element to the standard treatment, we could possibly reduce that rate even further," she said. The study is seeking 2,000 participants at multiple cancer centers across the country. Before taking part in the trial, interested participants will undergo a physical exam and a mammogram. Of those selected, one group will receive radiation therapy for three to six weeks as part of their regular treatment following surgery, while the other group will receive both radiation treatment and trastuzumab, which will be given through injection. Following treatment, participants will have follow-up physical exams and a mammogram each year for the next ten years. Women over age 18 who have been diagnosed with HER2-positive DCIS and have had a lumpectomy are eligible to participate, although other criteria also must be met. For more information on how to take part, individuals should call CINJ"s Office of Human Research Services at 732-235-8675. Clinical trials, often called cancer research studies, test new treatments and new ways of using existing treatments for cancer. At CINJ, researchers use these studies to answer questions about how a treatment affects the human body and to make sure it is safe and effective. There are several types of clinical trials currently underway at CINJ, including those that diagnose, treat, prevent, and manage symptoms of cancer. Many treatments used today, whether drugs or vaccines; ways to do surgery or give radiation therapy; or combinations of treatments, are the results of past clinical trials. As New Jersey"s only National Cancer Institute-designated Comprehensive Cancer Center, CINJ offers patients access to treatment options not available at other institutions within the state. CINJ currently enrolls more than 1,000 patients on clinical trials, including approximately 15 percent of all new adult cancer patients and approximately 70 percent of all pediatric cancer patients. Enrollment in these studies nationwide is fewer than five percent of all adult cancer patients. The Cancer Institute of New Jersey


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