Research & Clinical Trials

How better care is discovered

Research & clinical trials

Cancer research examines prevention, screening, biology, treatment, side-effect control, survivorship and health equity.

Researchers reviewing cancer laboratory results

What is a clinical trial?

A clinical trial is a carefully designed study involving people. It may test a new treatment, prevention method, diagnostic approach or way to improve quality of life.

Joining is voluntary. Informed consent explains purpose, procedures, possible risks and benefits, alternatives, privacy and the right to leave.

Trial phases

Phase 1

Focuses on safety, dose and how a treatment behaves in the body.

Phase 2

Studies whether a treatment shows activity and continues monitoring safety.

Phase 3

Compares a new approach with the current standard in a larger group.

Phase 4

Studies longer-term effects after approval and wider use.

Randomization

Assignment by chance helps groups remain comparable. Placebos are rarely used alone when effective treatment exists.

Oversight

Review boards, monitoring plans and safety rules protect participants.

Questions to ask

  • Why might this study fit my diagnosis?
  • What are standard alternatives?
  • What extra visits, tests or travel are required?
  • Which costs are covered, and what might insurance cover?
  • Who do I contact after hours?

Search verified registries

Use ClinicalTrials.gov and the National Cancer Institute trial search. Discuss any study with your oncologist and contact the listed research team to confirm current eligibility.

Search ClinicalTrials.govNCI trial search