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Clinical trials in ovarian carcinoma: requirements for standard approaches and regimens

T Thigpen1, G Stuart, A du Bois

  • 1Department of Medicine, Division of Oncology, University of Mississippi Medical Center, Jackson 39216, USA. JTTHIGPEN@worldnet.att.net

Annals of Oncology : Official Journal of the European Society for Medical Oncology
|October 22, 2005
PubMed
Abstract

No abstract available in PubMed .

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Clinical Trials01:16

Clinical Trials

Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
Clinical Trials: Overview01:11

Clinical Trials: Overview

Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...

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