You can always stop participating in the clinical trial at any time. For more information on cancer clinical trials or research studies, ask your medical care provider or call or send an email to winshipcto emory. Types of Clinical Trials A clinical trial is a form of research that enlists participants to help answer specific questions about new ways to prevent, diagnose, and treat cancer. Clinical trials occur in three phases necessary for FDA approval of a new treatment option:. Phase I Clinical Trial: Phase I trials study whether a new treatment is safe to use over a range of doses.
Phase I Unit at Winship. PROS: Cancer clinical trials offer high-quality cancer care. In cancer clinical trials if you do not receive the new treatment being tested, you will receive the best standard treatment.
This may be as good as, or better than, the new approach. If a new treatment approach is proven to work and you are taking it, you may be among the first to benefit. By looking at the pros and cons of cancer clinical trials and your other treatment choices, you are taking an active role in a decision that affects your life.
You may have the chance to help others and improve cancer treatment. CONS: New treatments in cancer clinical trials are not always better than standard care. You may have side effects that medical care providers do not expect or that are worse than those of standard treatment. By downloading Emory news media, you agree to the following terms of use: Creative Commons Attribution-NoDerivatives 4. Section 1 — Definitions. Adapted Material means material subject to Copyright and Similar Rights that is derived from or based upon the Licensed Material and in which the Licensed Material is translated, altered, arranged, transformed, or otherwise modified in a manner requiring permission under the Copyright and Similar Rights held by the Licensor.
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For purposes of this Public License, simply making modifications authorized by this Section 2 a 4 never produces Adapted Material. Downstream recipients. The focus of the CTO is to help develop and support institutional clinical research studies, particularly phase I and institutional studies.
In , the Phase I Clinical Trials Unit opened and is dedicated to advancing cancer research through a singular focus on caring for patients enrolled in phase I clinical trials. Additionally, support is provided at other area facilities where Emory investigators conduct clinical trials, including Atlanta VA Medical Center and Grady Memorial Hospital.
The CTO has supported clinical research from Emory University that has led to numerous publications since The CTO manages the overall process of subject screening, consent, registration, data entry and regulatory document submission and management for clinical research studies involving cancer patients.
To achieve the goals, the CTO pursues the following specific objectives:. The CTO is the central clearinghouse for the initiation and registration of clinical protocols involving cancer patients.
It is authorized by the executive director of the Winship Cancer Institute to:. The CTO has developed policies and procedures to facilitate centralized management of cancer clinical studies across all departments in which subjects may be enrolled on cancer clinical trials.
The CTO staff monitors study procedures to ensure regulatory compliance and provides regular instruction to new and current staff in these areas. The creation of these teams has stimulated greater interaction, communication and teamwork among the faculty and research staff facilitating clinical trials.
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