This site contains information about clinical trials sponsored by Novo Nordisk. It is not intended to replace the advice of a healthcare professional and should not be construed as providing advice or making a recommendation. The information on this site should not be relied on as the basis for any decision or action. Only a physician can determine whether a specific product is correct for a particular patient. If you have questions regarding any information contained on this site you should consult a physician.
A clinical trial is a research study where volunteers agree to test a new medicine.
The trial is designed to discover whether this new medicine works and if it is safe. It’s only through clinical trials and the help of volunteers like you that important questions about new medicines can be answered.
What are clinical trials for?
Clinical trials test potential new medicines to see:
- If the medicine works
- If there are safety concerns
- What the side effects are
Are clinical trials safe?
Strict rules about how to run a clinical trial were put in place to protect the rights, safety, privacy, and well-being of trial volunteers.
How are clinical trials set up?
Every clinical trial has a plan, also known as a protocol. The plan outlines the details of the trial, including which people may enrol, how long the trial will take, and how the results will be measured. Before the trial can start, an independent ethics committee and the local government’s health authorities must approve this plan.
Keep in mind, clinical trials will only take place if:
- There is a scientific and medical reason for the trial
- There are more benefits than risks for the trial volunteers
The 4 phases of clinical research
Before a medicine can be tested in a clinical trial, it must first be tested in animals to confirm that it is safe. Testing new medicines usually goes through the following 4 phases.
Phase I
Basic safety
These trials test a new medicine to see if it is safe. In this phase, a small number of people, who may be healthy, are given the medicine. When the safety profile of the new medicine has been established, the medicine can move to Phase II
Phase II
Does the medication work?
These trials test the new medicine on a larger group of people (usually a few hundred) with a specific disease for a longer time. This is done to see if or how the medicine works. This is also known as a medicine’s efficacy.
Phase III
Testing in a larger group
These trials test medicines in even larger groups of people (typically several hundred) with a specific disease. This phase compares the new medicine to the usual medicine used for the disease, or to a placebo (dummy medicine that doesn’t have active ingredients).
Doctors will often use the “blinded” method for Phase II and Phase III trials. This means that neither the participant nor the doctor will know which medicine or placebo the volunteer receives.
Phase IV
Post-approval testing
In these trials, the medicine tested has already been approved for use. Phase IV trials include the largest group of participants (usually several hundred to thousands of volunteers). Phase IV trials are sometimes called Post Marketing Surveillance Trials.
Want to know more?
Find out more about what it may be like to participate in a clinical trial.
What it may be to participate in a clinical trial
What is a clinical trial?
It’s important to attend every clinical visit so the trial team can better understand the results.
What is a clinical trial?
You will be monitored closely and your team will be available for questions and support.
What is a clinical trial?
You can join a trial at any phase.
What is a clinical trial?
Clinical trials are one of the most important steps to finding new medicines.
Questions or concerns
Do you have any question about what it’s like being a clinical volunteer? Have a look at our answers to frequently asked questions.
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March 2024