FAQS

A clinical trial is a research trial conducted in human volunteers to answer specific health questions. Interventional trials determine whether experimental treatments or new ways of using known therapies are safe and effective under controlled environments.

NSCLC trials seek to evaluate the safety, tolerability, and efficacy of an investigational treatment in treating NSCLC.

Eligibility will differ based on which NSCLC trial you join.

If you join one of the trials, there are certain things you will be expected to do. This includes attending study visits and undergoing certain assessments and procedures including chest X-rays, imaging scans, biopsies, and blood draws.

The length of your participation will depend on several factors, including which trial you join in and your response to the study treatment. Your participation may last up to 5 years.

You may benefit from additional check-ups on top of your regular care, and you may have access to NSCLC specialists. There is no guarantee that you will receive a medical benefit from participating in one of these trials. Your condition may get better, stay the same, or may even get worse.

As with all treatments, there are possible risks and side effects when taking them. You will be provided with an Informed Consent Form that will explain the risks that have been seen in other clinical trials researching the investigational study treatment. It is also possible that the treatment may affect you in unknown ways. If you should experience any changes in your health, however unrelated you think they may be, you should tell your study doctor and study team.

The NSCLC trials are taking place at study centers worldwide. Find the study center closest to you by using our site finder tool.