Clinical research trials are studies that evaluate how well a new medical treatment performs by testing it on a select group of patients. Clinical trials are conducted according to a protocol that describes the types of patients who may enter the study, the schedules of tests and procedures, drugs, dosages, the length of the study and how the outcomes will be measured.

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If treatment for your disease isn't available or if the standard treatment hasn't worked for you, you might consider a clinical trial. Clinical trials can provide access to new or experimental treatments that otherwise aren't available. Each person who participates in the study must agree to the rules set out by the protocol. All our studies are performed under the guidelines of the FDA’s Code of Federal Regulations and ICH Good Clinical Practice Standards.

Please contact our Clinical Research Department at 678-741-5000 to go over your medical history with one of our experienced Clinical Research Coordinators. If you meet criteria for any trials, you may be able to receive the latest treatment that science has to offer at no charge to you. Please know that this is a voluntary decision, and at any time you have the right to withdraw your consent for any reason.

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