By participating in a research trial, you help researchers better understand how investigational medications work and support research that may lead to future treatment options. You may also have access to investigational treatment under physician supervision at no cost before it is widely available.

After you express interest in a study, a member of the research team may call you to ask questions to determine whether you might qualify. If you meet the initial eligibility criteria, you may be invited to attend a screening visit. During this visit, the study will be reviewed with you in detail, and you will be asked to provide informed consent before any study-specific procedures or assessments are conducted. If you are eligible and decide to participate, you may enroll in the trial.

Informed consent is the process of providing you with detailed information about a clinical trial so you can decide whether participation is right for you. A member of the research team will review the study with you, including the purpose of the trial, the investigational treatment being studied, required procedures, potential risks and benefits, alternative treatment options, and your right to withdraw at any time. You will have the opportunity to ask questions before deciding whether to participate. If you choose to enroll, you will be asked to sign an informed consent form before any study procedures begin. If new information becomes available during the trial, you will be informed and may be asked to review and sign an updated consent form.

A clinical trial is designed to determine whether an investigational treatment is safe and effective. Depending on the study, participants may receive the investigational treatment, a placebo, or the current standard of care. A placebo does not contain active medication. Throughout the study, the research team will monitor participants according to the study plan.

Compensation may be available for participating in a clinical trial. The amount and type of compensation, if offered, varies by study and may be based on factors such as time and commitment, travel, and study-related activities. Details about compensation will be provided during the informed consent process.

Clinical trials are conducted under federal regulations and are reviewed by Institutional Review Boards (IRBs) to help protect participants’ rights and safety. Participation may involve risks, including possible side effects from investigational treatments or study-related procedures. The research team will monitor your health throughout the study and will discuss potential risks with you during the informed consent process. If side effects occur, appropriate medical care will be available.

You can contact the research team to let them know you are interested in participating in a clinical trial.

During the screening visit, the research team will review the study requirements with you and confirm your eligibility. This may include a physical examination, collection of blood and urine samples, and other study-related tests or assessments. These procedures help determine whether the study is appropriate for you. If you meet the eligibility criteria and choose to participate, you may enroll in the trial.