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Are all studies the same?

Each year, millions of people volunteer to participate in clinical trials. These trials are a key part to developing new and improved therapies and treatments for disease.

Clinical studies are categorised into four different groups or phases. As a study medication goes through each phase, researchers begin to know more about the medication, how patients respond to the medication and any possible adverse reactions to the medications. Each phase has strict regulations about how studies are to be conducted.

Phase I Studies

are when a drug is tested in humans for the first time. The testing at this phase looks at the safety of a treatment as well as assessing dosing levels. These studies are generally done with a small group of volunteers over a certain time period. 

Phase II Studies

test the efficacy of a treatment – or how well it works. These studies are done with a larger group of volunteers. There may be multiple doses of medication being investigated as well as further safety assessments. 

Phase III Studies

are larger scale studies which involve several thousands of volunteer patients. Phase III studies allow researchers to gain a better understanding of the benefits and possible side effects to the treatments over a longer period of time. After successfully completing the Phase III trials, the company can submit the study information to get approval to market the treatment.

Phase IV Studies

are conducted after a treatment has been approved for sale. Phase IV allows companies and researchers to continue to monitor the treatment as well evaluate how it compares to other treatments.

Who can participate in a clinical trial?

Each clinical trial uses a different criteria for study involvement, including but not limited to age, disease type, current treatments etc. Our research team will assess all participants on a case by case basis for eligibility.

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Frequently asked questions

I'd like to join a trial!

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