Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican Patients
The aim of this pilot clinical trial was to evaluate the safety of a new formulation of prolonged-release Pirfenidone (PR-PFD) in chronic kidney disease (CKD), specifically focal and segmental glomerular hyalinization (FSGH). Open-label, pilot, nonrandomized trial. Eighteen patients previously diag...
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doaj-2af6ef8cbf7f48da87aa78b37d0f27862020-11-25T03:46:09ZengCodon PublicationsJournal of Renal and Hepatic Disorders2207-37442020-05-014110.15586/jrenhep.2020.61Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican PatientsSimón A. Ojeda-Duran 0Iván Lyra-Gonzalez 1Alejandra Meza-Rios2Silvia Lucano-Landeros3Ana Sandoval-Rodriguez4Monica Vazquez-Del Mercado5Arturo Santos6Lucia Flores-Contreras7Juan Armendáriz-Borunda8Hospital Real San José, Zapopan, Jalisco, Mexico.Institute of Molecular Biology in Medicine and Gene Therapy, CUCS, University of Guadalajara, Guadalajara, Jalisco, Mexico.Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Campus Guadalajara, Zapopan, Jalisco, Mexico.Institute of Molecular Biology in Medicine and Gene Therapy, CUCS, University of Guadalajara, Guadalajara, Jalisco, Mexico.Institute of Molecular Biology in Medicine and Gene Therapy, CUCS, University of Guadalajara, Guadalajara, Jalisco, Mexico.IIRSME, CUCS, University of Guadalajara, Guadalajara, Jalisco, Mexico.Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Campus Guadalajara, Zapopan, Jalisco, Mexico.Department of Health Sciences, CUTonala, University of Guadalajara, Tonala, Jalisco, Mexico.Institute of Molecular Biology in Medicine and Gene Therapy, CUCS, University of Guadalajara, Guadalajara, Jalisco, Mexico; Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Campus Guadalajara, Zapopan, Jalisco, Mexico. The aim of this pilot clinical trial was to evaluate the safety of a new formulation of prolonged-release Pirfenidone (PR-PFD) in chronic kidney disease (CKD), specifically focal and segmental glomerular hyalinization (FSGH). Open-label, pilot, nonrandomized trial. Eighteen patients previously diagnosed with CKD stages 1– 5 according to “Kidney Disease: Improving Global Outcomes” were enrolled in the study. Target dos-age of PFD was 1200 mg twice a day in the form of prolonged-release tablets to reach a full dosage of 2400 mg daily. Clinical trial was carried out for 60 months to evaluate the safety and efficacy of a newly formulated PR-PFD in patients with CKD. After the treatment for 60 months, it was found that PR-PFD kept renal function from declining significantly in CKD patients, as the glomerular filtration rate (GFR) showed only minimal variations throughout the study. Estimated glomerular filtration rate (eGFR) showed no differences at both baseline and the end points. Proteinuria improved, and creatinine, cystatin C, urea, hemoglobin and hepatic transaminases remained constant without any considerable changes across the study. Minor side effects were noticed when compared with those found in previous studies, indicating an increased tolerance to this pharmaceutical formulation of PFD. Prolonged-released PFD could be safely used as an adjuvant therapy in patients with CKD. Registry number was obtained from ClinicalTrials.gov (NCT02408744). https://jrenhep.com/index.php/jrenhep/article/view/61Chronic Kidney Diseaseglomerular filtration rateprolonged-released Pirfenidone. |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Simón A. Ojeda-Duran Iván Lyra-Gonzalez Alejandra Meza-Rios Silvia Lucano-Landeros Ana Sandoval-Rodriguez Monica Vazquez-Del Mercado Arturo Santos Lucia Flores-Contreras Juan Armendáriz-Borunda |
spellingShingle |
Simón A. Ojeda-Duran Iván Lyra-Gonzalez Alejandra Meza-Rios Silvia Lucano-Landeros Ana Sandoval-Rodriguez Monica Vazquez-Del Mercado Arturo Santos Lucia Flores-Contreras Juan Armendáriz-Borunda Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican Patients Journal of Renal and Hepatic Disorders Chronic Kidney Disease glomerular filtration rate prolonged-released Pirfenidone. |
author_facet |
Simón A. Ojeda-Duran Iván Lyra-Gonzalez Alejandra Meza-Rios Silvia Lucano-Landeros Ana Sandoval-Rodriguez Monica Vazquez-Del Mercado Arturo Santos Lucia Flores-Contreras Juan Armendáriz-Borunda |
author_sort |
Simón A. Ojeda-Duran |
title |
Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican Patients |
title_short |
Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican Patients |
title_full |
Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican Patients |
title_fullStr |
Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican Patients |
title_full_unstemmed |
Evaluation of Safety of a Newly Formulated Pirfenidone in Chronic Kidney Disease: A Non-Randomized Pilot Study in Mexican Patients |
title_sort |
evaluation of safety of a newly formulated pirfenidone in chronic kidney disease: a non-randomized pilot study in mexican patients |
publisher |
Codon Publications |
series |
Journal of Renal and Hepatic Disorders |
issn |
2207-3744 |
publishDate |
2020-05-01 |
description |
The aim of this pilot clinical trial was to evaluate the safety of a new formulation of prolonged-release Pirfenidone (PR-PFD) in chronic kidney disease (CKD), specifically focal and segmental glomerular hyalinization (FSGH). Open-label, pilot, nonrandomized trial. Eighteen patients previously diagnosed with CKD stages 1– 5 according to “Kidney Disease: Improving Global Outcomes” were enrolled in the study. Target dos-age of PFD was 1200 mg twice a day in the form of prolonged-release tablets to reach a full dosage of 2400 mg daily. Clinical trial was carried out for 60 months to evaluate the safety and efficacy of a newly formulated PR-PFD in patients with CKD. After the treatment for 60 months, it was found that PR-PFD kept renal function from declining significantly in CKD patients, as the glomerular filtration rate (GFR) showed only minimal variations throughout the study. Estimated glomerular filtration rate (eGFR) showed no differences at both baseline and the end points. Proteinuria improved, and creatinine, cystatin C, urea, hemoglobin and hepatic transaminases remained constant without any considerable changes across the study. Minor side effects were noticed when compared with those found in previous studies, indicating an increased tolerance to this pharmaceutical formulation of PFD. Prolonged-released PFD could be safely used as an adjuvant therapy in patients with CKD.
Registry number was obtained from ClinicalTrials.gov (NCT02408744).
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topic |
Chronic Kidney Disease glomerular filtration rate prolonged-released Pirfenidone. |
url |
https://jrenhep.com/index.php/jrenhep/article/view/61 |
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