Clinical trials
CLÍNICA UNIVERSIDAD DE NAVARRA PARTICIPATES IN, MANAGES AND PROMOTES A LARGE NUMBER OF CLINICAL TRIALS.
Through the Research Management Service, you can access the services that CUN can offer in clinical research.
CUN as a promoter and participating centre
The University of Navarra Clinic (CUN) has initiated and promoted numerous clinical trials. One of its priorities is to carry out clinical trials, whether they are promoted by the pharmaceutical industry or by the Clinic's own researchers. That is why we are at the disposal of laboratories wishing to carry out any of the phases that a clinical trial must go through essay .
In many cases, it will be a product that has been developed by the Unit at development of the medicine.
The number of clinical trials has increased exponentially in recent years. The number of sponsors who trust in the Clínica has also grown over time, a true reflection of the efforts made to become a benchmark centre in research and innovation.
More than 1,000 patients at the Clínica participate each year in the more than 100 clinical trials currently active, promoted both by the Clínica and by the most prestigious laboratories.
Clinical trials are mainly focused on the most prevalent pathologies, in line with the lines of research developed jointly between the Clinic and the CIMA.
Trials in the Clínica Universidad de Navarra | Phase I | Phase II | Phase III | Phase IV |
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Healthy volunteers Safety of the medicinal product |
Limited number of patients Preliminary safety data Benefit of the treatment |
Largest number of patients Safety and efficacy data |
Product on the market Measures long-term effects data |
|
Unit Phase I |
UCICEC - EECC Management |
Phase I | Healthy volunteers Safety of the medicinal product |
Phase II | Limited number of patients Preliminary safety data Benefit of the treatment |
Phase III | Largest number of patients Safety and efficacy data |
Phase IV | Product on the market Measures long-term effects data |
procedure
The Research Management Service will manage the administrative and legal issues related to the clinical trials of the Clínica Universidad de Navarra.
We have several models of contracts for conducting clinical trials. The models are flexible and can be adapted to each promoter and each study subject .
In parallel with the management of the contract, the following documentation will be required:
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Civil Liability Policy
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report economic
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Power of attorney (depending on the case)
In order to obtain the agreement of the centre, the promoter must send the following documentation:
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protocol
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Informed Consent/Patient Information Sheet
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report Detailed Economic
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Favourable opinion of the ECIC
contact
Clinical trial management
eecc@unav.esAvda. Pio XII, 53
31008 Pamplona, Spain
+34 948 176 748