WHO ICTRP trial

Clinical Trial to evaluate the effectivity and efficiency of preemptive…

EUCTR2019-000376-41-ES · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2019-000376-41-ES
Public title Clinical Trial to evaluate the effectivity and efficiency of preemptive genotyping before treatment with voriconazole
Scientific title Randomized and multicenter clinical trial to evaluate the effectiveness and efficiency of a voriconazole preemptive genotyping strategy in patients with risk of aspergillosis.
Primary sponsor Fundación de Investigación del Hospital Universitario La Paz (FIBHULP)
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes
Countries Spain
Conditions Invasive fungal disease in the hematologic patient. MedDRA version: 20.0 Level: HLGT Classification code 10017528 Term: Fungal infectious disorders System Organ Class: 10021881 - Infections and infestations MedDRA version: 20.0 Level: HLT…
Interventions Trade Name: Voriconazol Pharmaceutical Form: Powder for solution for injection/infusion INN or Proposed INN: VORICONAZOLE CAS Number: 137234-62-9
Registration date Dec 4, 2019
Target size 146
Secondary IDs VORIGENIPHARM
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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