Annual Report Vol 2 October 1 1986 September 30 1987 Part Ii Individual Project Reports Classic Reprint

Author : U. S. National Cancer Institute
Publisher : Forgotten Books
ISBN 13 : 9780484507202
Total Pages : 666 pages
Book Rating : 4.5/5 (72 download)

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Download or read book Annual Report, Vol. 2 written by U. S. National Cancer Institute and published by Forgotten Books. This book was released on 2017-12-23 with total page 666 pages. Available in PDF, EPUB and Kindle. Book excerpt: Excerpt from Annual Report, Vol. 2: October 1, 1990 Through September 30, 1991 The Cancer Therapy Evaluation Program (ctep) is responsible for the administration and coordination of the majority of the extramural clinical trials Supported by oct. These programs include the activities of the Clinical Cooperative Groups, the Phase I and Phase II new agent development contractors, and the holders of investigator-initiated grants (roi and P01) relating to cancer treatment. Certain programs in developmental radiotherapy, such as high let radiation, are administered in the Radiation Research Program. The Phase I development of biologic response modifiers is handled by the Biological Research Modifiers Program. The Investigational Drug Branch (108) is responsible for sponsoring trials of new investigational drugs and of evaluating them for efficacy and toxicity. It does this by: 1) Coordinating and monitoring the trials of new agents developed by the oct; 2) Planning with members of the Clinical Investigations Branch (see below overall strategies for new agent studies in specific tumor types; 3) Regulating the distribution of investigational new drugs for which oct is the sponsor; 4) Maintain close contact and ongoing dialogue with the pharmaceutical industry in an attempt to ensure that new agent development proceeds in a coordinated way. The Clinical Investigations Branch (cib) is responsible for development and implementation of disease-oriented treatment strategies across the spectrum of human malignancies. In doing so, it provides management and oversight of the clinical cooperative group program. It manages the oncology portfolios of R01 and P01 grants. The Regulatory Affairs Branch (rab) monitors the conduct of clinical trials performed in the nci-supported clinical trials network. It also assures that clinical investigators using experimental agents are in compliance with federal regulations regarding the use of such agents. At the start of the clinical testing of each investigational gent, rab obtains Investigational New Drug (nda) exemption authorization from the Food and Drug Administration (fda) and maintains close communication with fda in all matters relating to experimental drug studies. About the Publisher Forgotten Books publishes hundreds of thousands of rare and classic books. Find more at www.forgottenbooks.com This book is a reproduction of an important historical work. Forgotten Books uses state-of-the-art technology to digitally reconstruct the work, preserving the original format whilst repairing imperfections present in the aged copy. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in our edition. We do, however, repair the vast majority of imperfections successfully; any imperfections that remain are intentionally left to preserve the state of such historical works.