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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.

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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.

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Trials in the Clínica Universidad de Navarra Phase I Phase II Phase III Phase IV

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

Phase I

Unit Phase I

Phase II

UCICEC - EECC Management

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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:

  • Civil Liability Policy

  • report economic

  • Power of attorney (depending on the case)

In order to obtain the agreement of the centre, the promoter must send the following documentation:

  • protocol

  • Informed Consent/Patient Information Sheet

  • report Detailed Economic

  • Favourable opinion of the ECIC

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contact

Clinical trial management

Avda. Pio XII, 53

31008 Pamplona, Spain

+34 948 176 748

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