Clinical Trials
A clinical trial is a research study that tests a medical treatment such as a drug, therapy, or procedure with the help of volunteers. Volunteers may be either healthy individuals or patients with medical conditions. These studies are conducted by doctors and clinical research staff to help understand if a drug is safe and works well for the people who need it, with the goal to improve people’s health and quality of life.
The study methods are designed to follow closely monitored protocols. These methods are reviewed and approved by regulatory agencies and ethics committees. Your participation may help you as well as future patients receive better care and treatment options.
We are recruiting volunteers for clinical trials across a range of cancers, including blood cancers, lung cancer, gastrointestinal cancers, breast cancer, and other solid tumors.
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a clinical trial?
We are here to answer any questions you may have about participating in one of our clinical trials.
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Below are answers to frequently asked questions about clinical trials.
Why should you participate in a clinical trial?
Participating in a clinical trial might give you access to an investigational treatment, which can be especially important if current treatments do not work well for your medical condition. You also would play an active role in your own healthcare. Additionally, the study may help doctors learn more about cancer and help other people in the future. You should always discuss your potential participation with your doctor.
Why are clinical trials important?
Clinical trials are essential for advancing medical knowledge and improving patient care. They help doctors find better ways to understand, prevent, diagnose, and treat medical conditions. Most medicines available today are the result of volunteers participating in clinical trials driven by patients needing additional treatment options. Although there is no guarantee of personal benefit, participation contributes valuable knowledge that may help future volunteers or patients.
How do clinical trials work?
Clinical trials follow a specific plan called a protocol. This plan explains how the clinical trial will be conducted, who can participate, and how study participants will be monitored for safety. Additionally, clinical trials must follow strict guidelines set by regulatory agencies and ethics committees to ensure protection of participants and require a participant to sign an “Informed Consent” form. The informed consent process for clinical trials makes sure that study participants understand the study’s purpose, risks, and potential benefits before agreeing to participate. Study participants are carefully checked throughout a clinical trial. They have regular checkups to track their health and any responses to the treatment.