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      <image:title>About - Clinical Trials</image:title>
      <image:caption>Clinical trials are at the heart of all medical advances. Clinical trials are medical research studies that are conducted to investigate the safety and efficacy of potential new drugs and medical treatments, also referred to as investigational drugs, as well as their side effects and uses. Investigational drugs are not yet approved by the U.S. Food and Drug Administration (FDA) to be prescribed. Clinical trials contribute to the development of medical knowledge and advancement of patient care. Clinical trials can provide another treatment option to patients in addition to standard therapies.</image:caption>
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      <image:caption>In a clinical trial, participants are provided investigational medication under physician and other research professional supervision. The U.S. Department of Health and Human Services (HHS) and the Food and Drug Administration (FDA) ensure that clinical trials adhere to federal regulations to protect participants. Clinical trials are also overseen by an Institutional Review Board (IRB), or an ethics committee, who prioritize participant safety, welfare, and rights.</image:caption>
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