Psoriasis Clinical Trials California
by admin on Saturday, February 26th, 2011 | No Comments
Psoriasis Clinical Trials California
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Moderate-to-Severe Psoriasis $230 Written by experts in the dermatology field, the new Third Edition of Moderate-to-Severe Psoriasis discusses the current use of biologics and new pharmacologic and phototherapy treatments for moderate-to-severe psoriasis. With 80 high quality color figures and full color throughout, this stand-alone text emphasizes safe and effective treatments for the psoriasis patient that are perfect for the dermatologist in daily practice. New to the Third Edition : the addition of chapters on the use of infliximab, efalizumab, and Humera, as well as the latest status of clinical trials the most up-to-date phototherapy and laser treatment modalities stronger coverage of psoriatic arthritis |
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Textbook of Psoriasis $238.95 Your concise and manageable guide to psoriasis During the last decade, research into molecular genetics, inflammatory mechanisms and immunology has dramatically enhanced our insight into the pathogenesis of psoriasis, paralleled by a proliferation in therapeutic treatments. For those unable to keep pace with the continual volume of research on psoriasis, Textbook of Psoriasis provides a concise and digestible account of the subject. Aimed at both the trainee and practising dermatologist, Textbook of Psoriasis concentrates mainly on the clinical presentation of psoriasis and the management of the condition using the latest pharmacological agents. In addition, it also reviews the underlying science from the point of view of causation and pathology. Containing contributions from a distinguished team of experts, the book remains in three sections which discuss the clinical morphology of the skin, its etiology and pathogenesis, and finally the current available treatments for this distressing disease. |
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Clinical Trials $79.95 Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines is a practical guidebook for those engaged in clinical trial design. This book details the organizations and content of clinical trials, including trial design, safety, endpoints, subgroups, HRQoL, consent forms and package inserts. It provides extensive information on both US and international regulatory guidelines and features concrete examples of study design from the medical literature. This book is intended to orient those new to clinical trial design and provide them with a better understanding of how to conduct clinical trials. It will also act as a guide for the more experienced by detailing endpoint selection and illustrating how to avoid unnecessary pitfalls. This book is a straightforward and valuable reference for all those involved in clinical trial design. Provides extensive coverage of the "study schema" and related features of study design Offers a "hands-on" reference that contains an overview of the process, but more importantly details a step-by-step account of clinical trial design Features examples from the medical literature to highlight how investigators choose the most suitable endpoint(s) for clinical trial and includes graphs from real clinical trials to help explain each concept in study design Integrates clinical trial design, pharmacology, biochemistry, cell biology and legal aspects to provide readers with a comprehensive look at all aspects of clinical trials |
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Handbook of Psoriasis $104.95 The new second edition of the Handbook of Psoriasis remains an easy-to-read but detailed text on a common skin disease which affects 2% of the world's population. The text is designed as a reference for both the specialist and the primary care physician and can be read cover-to-cover in a week. Each chapter stands alone as a reference to a specific topic but is clearly cross-referenced to offer a more detailed perspective. This new edition runs the full gamut from pathogenesis to clinical variants of psoriasis to individual treatments with emphasis on standard protocols. Each chapter has been carefully updated to reflect developments in the last five years and new chapters cover such topics as childhood psoriasis, psoriatic arthritis and biologic immunotherapy. |
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Treatment of Psoriasis $169 Psoriasis is an inherited skin disease that has been diagnosed in 4.5 million adults in the United States. About 10 percent to 30 percent of people with psoriasis also develop psoriatic arthritis, which causes pain, stiffness and swelling in and around the joints. The book reviews the clinical manifestations of these two entities. The main focus is on the evolving paradigm of therapy. Topical and ultraviolet therapy are discussed first, followed by traditional systemic therapy. A major focus is on biologic therapies. New agents in development are also reviewed. The book concludes with an evaluation of the quality of life impact of this disease. This volume provides an in-depth overview of the current state of psoriasis and its management. It is of interest to clinicians, researchers, and even patients who wish to learn more. It is also of interest to those in the pharmaceutical industry, and those in finance who cover the pharmaceutical field. |
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Advances in Clinical Trials Biostatistics $109.95 From aspects of early trials to complex modelling problems, this reference summarizes methodology used in the design and analysis of clinical trials. Chapters have been contributed by international methodologists experienced in clinical trials practice. |
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Cancer Clinical Trials $129 Clinical trials remain the most important vehicle for improving the care of cancer patients. This book presents the fundamental components and challenges involving clinical investigations. It aims to bring the issues of cancer clinical trials into focus so that proactive strategies may be developed to make such trials more user-friendly. |
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Randomized Clinical Trials $79 Using examples and case studies from industry, academia and research literature, Randomized Clinical Trials provides a detailed overview of the key issues involved in designing, conducting, analysing and reporting randomized clinical trials.? It examines the methodology for conducting Phase III clinical trials, developing the protocols, the practice for capturing, measuring, and analysing the resulting clinical data and their subsequent reporting. Randomized clinical trials are the principal method for determining the relative efficacy and safety of alternative treatments, interventions or medical devices.? They are conducted by groups comprising one or more of pharmaceutical and allied health-care organisations, academic institutions, and charity supported research groups.? In many cases such trials provide the key evidence necessary for the regulatory approval of a new product for future patient use.? Randomized Clinical Trials provides comprehensive coverage of such trials, ranging from elementary to advanced level. Written by authors with considerable experience of clinical trials, Randomized Clinical Trials is an authoritative guide for clinicians, nurses, data managers and medical statisticians involved in clinical trials research and for health care professionals directly involved in patient care in a clinical trial context. |
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Mild-to-Moderate Psoriasis $230 Using a practical and problem-focused approach, this updated, full-color Second Edition of Mild-to-Moderate Psoriasis equips dermatologists, internists, family practitioners, and residents with a state-of-the-art guide to the clinical management of mild-to-moderate psoriasis. Written by an international team of key opinion leaders, this resource explores new treatments for the condition and provides clinicians with up-to-date management strategies for optimum patient management. New to the Second Edition : updates on topical corticosteroids, calcipotriene, tazarotene, tars, anthralin, salicylic acid, and phototherapy new treatments such as tazarotene gel, scalp psoriasis treatment, topical vitamin D, and analogs chapters devoted to lasers and adhesive patches expanded coverage on scalp psoriasis |
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Design and Analysis of Clinical Trials $199 Praise for the First Edition of Design and Analysis of Clinical Trials "An excellent book, providing a discussion of the clinical trial process from designing the study through analyzing the data, and to regulatory requirement . . . could easily be used as a classroom text to understand the process in the new drug development area." – Statistical Methods in Medicine A complete and balanced presentation now revised, updated, and expanded As the field of research possibilities expands, the need for a working understanding of how to carry out clinical trials only increases. New developments in the theory and practice of clinical research include a growing body of literature on the subject, new technologies and methodologies, and new guidelines from the International Conference on Harmonization (ICH). Design and Analysis of Clinical Trials , Second Edition provides both a comprehensive, unified presentation of principles and methodologies for various clinical trials, and a well-balanced summary of current regulatory requirements. This unique resource bridges the gap between clinical and statistical disciplines, covering both fields in a lucid and accessible manner. Thoroughly updated from its first edition, the Second Edition of Design and Analysis of Clinical Trials features new topics such as: Clinical trials and regulations, especially those of the ICH Clinical significance, reproducibility, and generalizability Goals of clinical trials and target population New study designs and trial types Sample size determination on equivalence and noninferiority trials, as well as comparing variabilities Also, three entirely new chapters cover: Designs for cancer clinical trials Preparation and implementation of a clinical protocol Data management of a clinical trial Written with the practitioner in mind, the presentation assumes only a minimal mathematical and statistical background for its reader. Instead, the writing emphasizes real-life examples and illustrations from clinical case studies, as well as numerous references-280 of them new to the Second Edition-to the literature. Design and Analysis of Clinical Trials , Second Edition will benefit academic, pharmaceutical, medical, and regulatory scientists/researchers, statisticians, and graduate-level students in these areas by serving as a useful, thorough reference source for clinical research. |
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Statistics Applied to Clinical Trials $119 Explains classical statistical analysis of clinical trials. This book addresses relatively novel issues, including equivalence testing, interim analysis, sequential analysis, meta-analysis, and provides a framework of the best statistical methods available for such purpose. It is suitable for investigators in the field of clinical trials. |
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Data Monitoring in Clinical Trials $74.95 Randomized clinical trials are the gold standard for establishing many clinical practice guidelines. Therefore, trials must be monitored. Frequently, a group of external experts is charged with this monitoring responsibility. This book, through a series of case studies, illustrates the complexity of this monitoring process. |
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Sample Sizes for Clinical Trials $79.95 Featuring worked examples and problems based on real-world scenarios, this book takes readers through the process of calculating the sample size for various types of clinical trials. It covers the most common types of clinical trials across different phases. It discusses how assumptions made in a sample size calculation can impact the calculation. |
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Data and Safety Monitoring Committees in Clinical Trials $89.95 Data and Safety Monitoring Committees in Clinical Trials |
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Management of Data in Clinical Trials $146 A valuable new edition of the trusted, practical guide to managing data in clinical trials Regardless of size, type, or complexity, accurate results for any clinical trial are ultimately determined by the quality of the collected data. Management of Data in Clinical Trials, Second Edition explores data management and trial organization as the keys to developing an accurate and reliable clinical trial. With a focus on the traditional aspects of data collection as well as recent advances in technology, this new edition provides a complete and accessible guide to the management structure of a clinical trial, from planning and development to design and analysis. Practical approaches that result in the collection of complete and timely data are also provided. While maintaining a comprehensive overview of the knowledge and tools that are essential for the organization of a modern clinical trial, the author has expanded the topical coverage in the Second Edition to reflect the possible uses of recent advances in technology in the data collection process. In addition, the Second Edition discusses the impact of international regulations governing the conduct of clinical trials and provides guidelines on ensuring compliance with national requirements. Newly featured topics include: The growing availability of "off-the-shelf" solutions for clinical trials Potential models for collaboration in the conduct of clinical trials between academia and the pharmaceutical industry The increasing use of the Internet in the collection of data and management of trials Regulatory requirements worldwide and compliance with the ICH Good Clinical Practice (GCP) Guidelines Development of Standard Operating Procedures for the conduct of clinical trials Complete with chapter summaries that reinforce key points as well as over one hundred examples, Management of Data in Clinical Trials, Second Edition is an ideal resource for practitioners in the clinical research community who are involved in the development of clinical trials, including data managers, research associates, data coordinators, physicians, and statisticians. This book also serves as an excellent supplemental text for courses in clinical trials at both the undergraduate and graduate levels. |
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A Concise Guide to Clinical Trials $61.95 Clinical trials have revolutionized the way disease is prevented, detected and treated, and early death avoided, and they continue to be an expanding area of research. They are central to the work of pharmaceutical companies, and there are many academic and public sector organizations that conduct trials on a wide variety of interventions, including drugs, devices, surgical techniques, and changes in behaviour and lifestyle. A Concise Guide to Clinical Trials provides a comprehensive yet easy-to-read overview of the design, conduct and analysis of trials. It requires no prior knowledge on the subject as the important concepts are introduced throughout. There are chapters that distinguish between the different types of trials, and an introduction to systematic reviews, health-related quality of life and health economic evaluation. The book also covers the ethical and legal requirements in setting up a clinical trial due to an increase in governance responsibilities and regulations. This practical guidebook is ideal for busy clinicians and other health professionals who do not have enough time to attend courses or search through extensive textbooks. It will help anyone involved in undertaking clinical research, or those reading about trials. The book is aimed at: Those wishing to learn about clinical trials for the first time, or as a quick reference guide, for example as part of a taught course on clinical trials Health professionals who wish to conduct their own trials, or participate in other people’s studies People who work in pharmaceutical companies, grant funding organisations, or regulatory agencies |
