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Randomized, phase 1/2, double-blind pioglitazone repositioning trial combined with antifungals for the treatment of cryptococcal meningitis – PIO study

BACKGROUND: Cryptococcosis affects more than 220,000 patients/year, with high mortality even when the standard treatment [amphotericin B (AMB), 5-flucytosin (5-FC) and fluconazole] is used. AMB presents high toxicity and 5-FC is not currently available in Brazil. In a pre-clinical study, pioglitazon...

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Detalles Bibliográficos
Autores principales: Gouveia-Eufrasio, Ludmila, Ribeiro, Noelly Queiroz, Santos, Julliana Ribeiro Alves, da Costa, Marliete Carvalho, Emídio, Elúzia Castro Peres, de Freitas, Gustavo José Cota, do Carmo, Paulo Henrique Fonseca, Miranda, Bárbara Alves, de Oliveira, João Carlos Maia Dornelas, da Silva, Lívia Mara Vitorino, Teixeira Leocádio, Victor Augusto, Randi Magalhães, Vanessa Caroline, Penido, Indiara, Pereira, Leonardo Soares, Rabelo, Lívia Frota, de Almeida Faria, Flávio Augusto, Teixeira Dutra, Maria Rita, Aspahan, Maíra, de Paula, Ludmila, da Silva, Dirce Inês, Tavares Melo, Márcia Gregory, de Andrade Zambelli, Virginia Antunes, Gomes Faraco, André Augusto, da Costa César, Isabela, Alves, Glauciene Prado, da Cunha Melo, Lívia Fulgêncio, de Aguiar Peres, Nalu Teixeira, Santos, Daniel Assis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8099743/
https://www.ncbi.nlm.nih.gov/pubmed/33997457
http://dx.doi.org/10.1016/j.conctc.2021.100745
Descripción
Sumario:BACKGROUND: Cryptococcosis affects more than 220,000 patients/year, with high mortality even when the standard treatment [amphotericin B (AMB), 5-flucytosin (5-FC) and fluconazole] is used. AMB presents high toxicity and 5-FC is not currently available in Brazil. In a pre-clinical study, pioglitazone (PIO - an antidiabetic drug) decreased AMB toxicity and lead to an increased mice survival, reduced morbidity and fungal burden in brain and lungs. The aim of this trial is to evaluate the efficacy and safety of PIO combined with standard antifungal treatment for human cryptococcosis. METHODS: A phase 1/2, randomized, double blind, placebo-controlled trial will be performed with patients from Belo Horizonte, Brazil. They will be divided into three groups (placebo, PIO 15 mg/day or PIO 45 mg/day) and will receive an additional pill during the induction phase of cryptococcosis’ treatment. Our hypothesis is that treated patients will have increased survival, so the primary outcome will be the mortality rate. Patients will be monitored for survival, side effects, fungal burden and inflammatory mediators in blood and cerebrospinal fluid. The follow up will occur for up 60 days. CONCLUSIONS: We expect that PIO will be an adequate adjuvant to the standard cryptococcosis’ treatment. TRIAL REGISTRATION: ICTRP/WHO (and International Clinical Trial Registry Plataform (ICTRP/WHO) (http://apps.who.int/trialsearch/Trial2.aspx?TrialID=RBR-9fv3f4), RBR-9fv3f4 (http://www.ensaiosclinicos.gov.br/rg/RBR-9fv3f4). UTN Number: U1111-1226-1535. Ethical approvement number: CAAE 17377019.0.0000.5149.