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experienced by those starting with no knowledge of cancer nor how the FDA is intimately involved in the clinical aspects of a new treatment.;
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in tumors. An increasing number of compounds targeting specific molecules or cancer cells have been developed and, for some of them, approved by the;
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been approved by the FDA within the past year * Updated new indications for previously approved agents * Indications, drug doses and;
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of all the major cancers. Key Features: * Addition of 16 new agents and several new supplemental indications that have all been approved by;
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-estrogen drug approved in 2013 that is classified as a selective estrogen receptor modulator (SERM). Other SERMs approved by the FDA include;
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patient referral to post-therapy management in a concise and practical format. Providing clinical guidance on the implementation and management;
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details the preclinical and clinical development of the first FDA-approved cytotoxin. With a focus on clinical developmental approaches to the;
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in cancer and their alterations, which has enabled the emergence of a targeted (somewhat personalized) medicine approach to treatment. Today;
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benefit in a randomized Phase III trial. The combination of bevacizumab, the first FDA approved angiogenesis inhibitor, with cytotoxic regimens;
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benefit in a randomized Phase III trial. The combination of bevacizumab, the first FDA approved angiogenesis inhibitor, with cytotoxic regimens;
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This is a detailed and practical guide to botulinum neurotoxin therapy (BoNT) and the wide range of applications for neurological and pain;
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for the treatment of a serious condition, FDA may use one or more of its expedited programs, such as fast track and breakthrough therapy;
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Head and Neck Cancers: Evidence-Based Treatment presents a practical, state-of-the-art resource for any clinical oncologist treating or;
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support the FDA's review of prescription drugs. First, FDA reviews the safety and effectiveness of new drugs that manufacturers wish to market;
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therapy. These new breakthroughs, now approved by the FDA, are a part of multiple phase III international trials and ongoing research in malignant;
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Cancer Genomics for the Clinician is a practical guide to cancer genomics and its application to cancer diagnosis and care. The book begins;
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Drug Discovery in Cancer Epigenetics is a practical resource for scientists involved in the discovery, testing, and development;
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A brand-new title in the field of dermatology, Therapy for Severe Psoriasis provides the ultimate coverage of the treatment;
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by a companion diagnostic test. This book describes the ways in which FDA has worked to respond to, anticipate and help drive scientific;
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Gene therapy as a treatment for cancer is at a critical point in its evolution. Exciting new developments in gene targeting and vector;
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PARP Inhibitors for Cancer Therapy provides a comprehensive overview of the role of PARP in cancer therapy. The volume covers the history;
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Managing Cancer Breakthrough Pain is a comprehensive review of cancer breakthrough pain (cBTP) and rapid-onset opioids (ROO), the only;
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Kinase Inhibitor Drugs covers a wide and comprehensive range of topics about kinase-targeted inhibitors in cancer therapy, one of the;
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) (BoNT) dosage information is presented in an easy-to-navigate table format. The tables are organized by clinical indication along with each;
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The National Cancer Institute's (NCI) Clinical Trials Cooperative Group Program has played a key role in developing new and improved cancer;
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treatment of cancer. This is achieved by enhancing the bodys natural ability to fight cancer. In cancer immunotherapy, antibody proteins of the;
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ascension into the standard of care as first-line treatment for a growing number of disease settings. New to this edition are chapters with deeper;
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