Conducting Tirals

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The Clinical Research Institute coordinates and conducts a variety of clinical trials, including ones for the following therapeutic areas:

Vaccines In a clinical trial, participants receive specific interventions according to the research plan or protocol created by the investigators. These interventions may be medical products, such as drugs or devices; procedures; or changes to participants’ behavior, such as diet. Trials may compare a new medical approach to a standard one that is already available, to a placebo that contains no active ingredients or to no intervention. When a new product or approach is being studied, it is not usually known whether it will be helpful, harmful or no different than available alternatives (including no intervention). The investigators try to determine the safety and effectiveness of the intervention by measuring certain outcomes in the participants.

Why should I participate in a clinical study?

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We can only reach breakthroughs in treatment and care if people participate in the studies.

Participating is safe and can help you

Every clinical study is reviewed thoroughly before your doctor asks you to participate. Clinical trials carry some risks, but your doctor is required by law to explain the risks to you clearly and make sure that you understand them. If your doctor tells you about the risks of participating in the study, ask yourself, “What are the risks of not participating in the study?” Most of the time, if you balance the possible benefits from participating against the risks, it is about the same as the risks of not being in the study.

On the other hand, the study may be of a new drug or treatment that could help you. If you don’t participate, it may be years before you have a chance to try that drug.

Join a Study

Joining a clinical trial can increase your knowledge and understanding of your disease.

Understanding Clinical Trials

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Be one in a million.

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A prophylactic vaccine

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A prophylactic vaccine

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A prophylactic vaccine

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