What is clinical research? What are clinical trials?
Clinical research is the process of studying diseases, and developing medications to possibly prevent, treat, or help relieve symptoms caused by different medical conditions. Before a medicine can become widely available, it must be tested in a series of clinical trials, or clinical research studies. The medicine being studied or tested in a clinical trial is called an investigational medication.
Most clinical trials recruit volunteers to participate in the study. Those volunteers are closely monitored to follow the effects of an investigational medication on their health, and that information is used by health authorities to determine if the investigational medication is safe and effective, and if it should be approved for general medical use.
How do clinical trials work?
Clinical trials usually go through 3 phases before an investigational medication can be approved for general use:
VALIANT is a Phase 3 study
Why do people participate in clinical research studies?
Clinical trial participants can have an impact on the lives of others by helping researchers advance medical science, develop treatment options, and better understand the disease.
It's important to remember that clinical trials involve some risks:
- There may be limited information about the safety or effectiveness of an investigational medication, including whether it works at all, or what side effects it could cause.
- Participants may not see improvement, or improvement may take several months or more to appear.
- There is potential for a participant's condition to worsen.
For these reasons trial participants are screened carefully and monitored throughout the trial.
Some trial participants also feel the additional time and support they receive from study doctors and investigators during the study helps them learn more about their condition. Whatever the motivation for joining a study, participation is entirely voluntary, and participants can choose to leave the study at any time, for any reason, if they change their mind.Learn more about the VALIANT study, and see if it might be right for you
Understanding clinical research terms
Clinical research terminology can sometimes be confusing. We have created this glossary of clinical trial language to help you understand some of the key terms:
|Clinical trial participants||People who voluntarily consent to take part in a clinical trial and who meet all of the eligibility criteria.|
|Eligibility criteria||The requirements one must meet to participate in a clinical trial. These may include age, diagnosis, current and previous treatments, allergies, medical history, and other conditions.|
|Independent ethics committee (IEC) or institutional review board (IRB)||Independent committees made up of medical experts and the general public, who review, approve, and monitor all aspects of clinical research studies involving people. These groups ensure study protocols adhere to all relevant regulations, and that the rights and welfare of all participants are protected.|
|Informed Consent Form (ICF)||An important written document that is part of a larger consent discussion with the study team. The ICF describes the study, including study-related procedures, timelines, and potential risks and benefits. By signing the ICF, patients agree to participate. Parents or guardians must sign for minors to participate in a clinical trial, however the minor may be asked to sign a simplified “Assent Form” to show they understand what is being asked of them and that they are participating voluntarily.|
|Investigational medication or drug||The drug or medicine being studied in a clinical trial. Typically, this medication is not yet approved for general use for the condition being studied.|
|Study medication or drug||This term may be used to describe the investigational medication or other study treatment (such as placebo) that a participant may receive while in the study.|
|Open-label, open-label extension||In an open-label study, or open-label extension (continuation of the study) both the study team and the participant know which treatment group they have been assigned to, or which study treatment is being administered.|
|Single-blind||In a single-blind study, the study participant does not know the study treatment group they have been assigned to, but the study team does.|
|Double-blind||In a double-blind study, neither the participant nor the study team knows which study treatment group the participant has been assigned to, but the study team can find out in case of an emergency.|
|Placebo||A substance that looks like the investigational medication but has no active medicinal ingredients. Placebos are used to compare the effectiveness of the investigational medication against no treatment. This is important to correct for the “placebo effect” when people feel better because they think they're taking a medicine, even if the medicine does not do anything.|
|Protocol||A detailed plan describing the purpose of a study, how the study will be conducted, who can participate, the investigational medication that will be administered, and how the effects will be monitored.|
|Randomisation||Randomised clinical trials assign participants at random to groups or cohorts within the trial, with each group receiving a different study treatment regimen. The different regimens may include the investigational medication, a placebo, an alternative therapy, or some combination of them.
Randomisation is important in gathering clear, unbiased results. Not all studies involve placebos, alternative therapies, or randomisation. If a particular study is randomised, patients will be made aware before agreeing to participate.
|Study team, or study site team||The doctors, nurses, and other professionals who are conducting a study at a particular clinic or hospital. The doctors may also be referred to as investigators for the study.|