About the Clinical Trials
A clinical trial is a research study that explores whether a medical strategy, investigational treatment, or device is safe and effective for humans. All potential new treatments go through a set of clinical trial phases under controlled conditions.
- Phase I tests safety in humans by giving the treatment or drug to healthy volunteers.
- Phase II tests safety and effectiveness in patients living with the disease being studied.
- Phase III tests safety and confirms effectiveness in patients with the disease and studies a larger group of people than the Phase II trial.
- Phase IV tests the drug’s effect in various populations and any side effects associated with long-term use after it is approved.
When these phases are complete, regulatory agencies – for example, U.S. Food & Drug Administration (FDA) or the European Medicines Agency (EMA) – determine whether the treatment can be prescribed by physicians to patients.
People choose whether or not to participate in clinical trials for various reasons, including:
- Gaining early access to treatments being studied for safety and effectiveness
- Receiving expert medical care
- Contributing to medical research
- Potentially helping future generations of people