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Mesothelioma Clinical Trial: Studies
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Every day, researchers are working to find new and improved treatments for mesothelioma through clinical trials. If you've been diagnosed with mesothelioma, you may be considering whether participating in one of these studies is right for you. The questions and answers below provide some basic information to help you decide.
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All the government-funded clinical trials must have their trial protocols approved before they can begin. The law requires the researcher to completely inform the patient about the study’s treatments and tests, and their possible benefits and risks. This informed consent must be signed before the participant can take part in the trial.
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Clinical trials are vital in studying all aspects of medicine, not just cancer. The stakes may seem higher when researching medicines to treat cancer, but all new treatments (drugs and medical devices) must go through clinical trials before being approved by the FDA for general use.
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The sorafenib clinical trial is being conducted at clinics, hospitals and cancer centers in 11 states. For the complete list, see Phase II Study of Sorafenib, NCI Patient Information. If you are interested in participating, talk to your doctor about a referral or call the appropriate trial contact person mentioned in the facility list.
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In Phase II mesothelioma clinical trials, the mesothelioma drug is studies in a larger group. The primary purpose of these studies is to see how well the drug or treatment shrinks tumors in patients with specific types of cancer. The investigator will watch closely for side effects and will ... watch how the disease responds to the treatment.
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The study protocol is the written plan for how a clinical trial is to be conducted. It is what is submitted to the FDA before a new treatment can be studied. A protocol contains the following information:
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