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Observational Study of the Effectiveness of Funded Drugs for Genitourinary Tumors.

Recruitingn/aAges 18 Years - anyAllSpanish Oncology Genito-Urinary Group
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In plain words

What the trial is, and whether it could suit you

SOGUG-PRINCIS is a retrospective (regarding patient inclusion) and prospective follow-up, epidemiological, non-interventional, non-blinded, non-randomized, multicenter, national observational study with drugs. This study will collect data from patients with genitourinary tumors to analyze the effectiveness under routine clinical practice conditions of drugs recently approved for funding in the Spanish National Health System. In all cases, the decision to start treatment will be made prior to and independently of participation in the study, which will be limited to subsequently collecting the data necessary to assess the objectives of the study. This study will serve as a registry for genitourinary cancers. Every time a new drug will be authorized, a new subproject with a primary endpoint will be opened to recruitment. The substudy will try to validate with real-world data the endpoints

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * Patients ≥18 years old. * Patients granting the ICF unless exemption or exceptions mentioned below. * Histological diagnosis of malignant neoplasia originating in the genitourinary system: kidney, renal pelvis, ureter, bladder, prostate, testicle and germinal tissue of other locations, urethra, penis, or seminal vesicles. * Patients have started treatment with medications whose positive resolution of financing by the Spanish National Health System for the aforementioned tumors has been after January 1, 2023. * Patients have started treatment after the official publication of the positive resolution of financing of the drug under study by the National Health System. This restriction is intended to avoid interference of the study with the marketing authorization processes by the European Medicines Agency, and price and reimbursement negotiations by the Spanish health authorities. * Patients have received treatment at the participating center. Exclusion Criteria: * Patients previously treated at another centre who have subsequently been referred to one of the participating centres. In this case, the patient will be included in the centre where treatment was started, or in the second centre if the first is not part of this study. * Patients who do not meet any of the inclusion criteria. * Evidence of an express objection by the subject or his/her legal representative to participate in the study.
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What it tests

  • darolutamide
  • Nivolumab monotherapy
  • enfortumab vedotin
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Where

84 sites
Complejo Hospitalario Universitario de Albacete
Albacete, Spain
Hospital General Universitario de Alicante
Alicante, Spain
Hospital Universitario Torrecárdenas
Almería, Spain
Hospital Universitario Reina Sofía
Córdoba, Spain
Hospital Universitario Clínico San Cecilio
Granada, Spain
Hospital Universitario Virgen a de las Nieves
Granada, Spain
Hospital Universitario de Jaén
Jaén, Spain
Hospital Universitario Jerez de la Frontera
Jerez de la Frontera, Spain

…and 76 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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