Each research project consists of several phases, during which progressively more questions are answered.
A phase that determines the highest dose of a drug a patient can take without experiencing side effects. The safety of participants is paramount, which is why only a few dozen people take part in this phase.
This is the time for the first evidence of efficacy. The aim of this phase is to confirm that the investigational product works as expected and to determine the optimal dose. Several hundred people are already participating in the study.
At this stage, more than a thousand patients are already participating. Thanks to a large study population, the results are more reliable and allow for the assessment of a drug’s efficacy and safety in a broad population. This is a key step before the registration of a new therapy.
Concerns medicines already approved for use. It allows monitoring of their long-term effects, effectiveness in routine clinical practice, and any rare adverse reactions.
After receiving your application, we will contact you by phone. If we are currently conducting a clinical trial related to your condition, we will invite you for a consultation at our Centre.
During the appointment, our specialists will answer all your questions and discuss the available treatment options. Based on your health condition and the information provided, we will select the clinical trial that best meets your needs.
If we are not currently conducting a clinical trial suitable for you, we will keep your application and contact you when an opportunity arises to participate in a study tailored to your health condition.
