All study medications or interventions used in clinical research have been reviewed and approved by appropriate regulatory authorities and independent ethics committees before being studied in people. While no research study can guarantee safety, participant safety is closely monitored throughout the study by qualified medical professionals, and safety information is reviewed on an ongoing basis.

Yes. Participation in clinical research is completely voluntary. You may choose not to participate or may withdraw from a study at any time without penalty or loss of medical care or benefits to which you are otherwise entitled.

This depends on the study design. Some studies are “blinded,” meaning participants may receive the study medication or a placebo. The study design and what you may receive will be explained in detail during the informed consent process before you decide whether to participate.

Informed consent is a process in which the study team explains the purpose of the study, what participation involves, potential risks and benefits, and your rights as a research participant. You will have the opportunity to review this information, ask questions, and take time to decide whether participation is right for you.

All clinical research studies involve some level of risk. Known risks and possible side effects are described during the informed consent process. Your health and safety are monitored throughout the study, and you will be informed of any new information that may affect your willingness to continue participation.

Some studies may offer compensation for time, travel, or study-related expenses. Compensation, if offered, varies by study and will be explained before you decide whether to participate.

Reasonable efforts are made to protect your privacy and maintain the confidentiality of your personal and medical information in accordance with applicable laws and regulations. Details about how your information may be used or shared are explained during the informed consent process.

Each study has specific eligibility criteria, which may include factors such as age, medical history, and current health status. The research team can help determine whether a particular study may be appropriate for you.

If you are interested in learning more, you may contact our research team through our website or by phone. A member of the team will provide additional information and answer any questions you may have.

Participation in a clinical research study is not intended to replace your regular medical care. You should continue to see your primary care provider or treating physician as recommended. Study-related procedures are performed for research purposes and are not a substitute for standard medical care.