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...

Full description

Bibliographic Details
Main Authors: 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
Format: Article
Language:English
Published: Codon Publications 2020-05-01
Series:Journal of Renal and Hepatic Disorders
Subjects:
Online Access:https://jrenhep.com/index.php/jrenhep/article/view/61
id doaj-2af6ef8cbf7f48da87aa78b37d0f2786
record_format Article
spelling 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).  
topic Chronic Kidney Disease
glomerular filtration rate
prolonged-released Pirfenidone.
url https://jrenhep.com/index.php/jrenhep/article/view/61
work_keys_str_mv AT simonaojedaduran evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT ivanlyragonzalez evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT alejandramezarios evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT silvialucanolanderos evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT anasandovalrodriguez evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT monicavazquezdelmercado evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT arturosantos evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT luciaflorescontreras evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
AT juanarmendarizborunda evaluationofsafetyofanewlyformulatedpirfenidoneinchronickidneydiseaseanonrandomizedpilotstudyinmexicanpatients
_version_ 1724507473477369856