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Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis
BACKGROUND: A new prolonged-release formulation of potassium citrate and potassium bicarbonate, ADV7103, has been shown to improve metabolic control, palatability, and gastrointestinal safety in patients with distal renal tubular acidosis (dRTA) when compared to standard of care (SoC) treatments. Th...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172410/ https://www.ncbi.nlm.nih.gov/pubmed/33635379 http://dx.doi.org/10.1007/s00467-020-04873-0 |
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author | Bertholet-Thomas, Aurélia Guittet, Catherine Manso-Silván, Maria A. Joukoff, Sophie Navas-Serrano, Victor Baudouin, Véronique Cailliez, Mathilde Di Maio, Massimo Gillion-Boyer, Olivia Golubovic, Emilija Harambat, Jérôme Knebelmann, Bertrand Nobili, François Novo, Robert Podracka, Ludmila Roussey-Kesler, Gwenaëlle Granier, Luc-André |
author_facet | Bertholet-Thomas, Aurélia Guittet, Catherine Manso-Silván, Maria A. Joukoff, Sophie Navas-Serrano, Victor Baudouin, Véronique Cailliez, Mathilde Di Maio, Massimo Gillion-Boyer, Olivia Golubovic, Emilija Harambat, Jérôme Knebelmann, Bertrand Nobili, François Novo, Robert Podracka, Ludmila Roussey-Kesler, Gwenaëlle Granier, Luc-André |
author_sort | Bertholet-Thomas, Aurélia |
collection | PubMed |
description | BACKGROUND: A new prolonged-release formulation of potassium citrate and potassium bicarbonate, ADV7103, has been shown to improve metabolic control, palatability, and gastrointestinal safety in patients with distal renal tubular acidosis (dRTA) when compared to standard of care (SoC) treatments. The present work evaluates safety and efficacy of ADV7103 during 24 months. METHODS: Thirty pediatric and adult patients were included in an open-label extension study after a phase II/III trial. Safety and tolerability were assessed. Plasma bicarbonate and potassium levels, as well as urine parameters, were evaluated over time. Acceptability, adherence, and quality of life were also assessed. The evolution of clinical consequences of dRTA in the cohort was explored. RESULTS: There were 104 adverse events (AEs) reported, but only 9 gastrointestinal events observed in five patients (17%) were considered to be related to ADV7103 treatment. There were no AEs leading to treatment discontinuation. Plasma bicarbonate and potassium levels were in the normal ranges at the different visits, respectively, in 69–86% and 83–93% of patients. Overall adherence rates were ≥ 75% throughout the whole study in 79% patients. An average improvement of quality of life of 89% was reported at 24 months of study. CONCLUSIONS: Common AEs concerned metabolism and gastrointestinal disorders; the former being related to the disease. Less than half of the gastrointestinal AEs were related to ADV7103 treatment and they were mostly mild in severity. Metabolic parameters were maintained in the normal ranges in most patients. Patient satisfaction was high and adherence to treatment was good and remained stable. TRIAL REGISTRATION NUMBER: Registered as EudraCT 2013-003828-36 on the 3rd of September 2013. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-020-04873-0. |
format | Online Article Text |
id | pubmed-8172410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-81724102021-06-07 Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis Bertholet-Thomas, Aurélia Guittet, Catherine Manso-Silván, Maria A. Joukoff, Sophie Navas-Serrano, Victor Baudouin, Véronique Cailliez, Mathilde Di Maio, Massimo Gillion-Boyer, Olivia Golubovic, Emilija Harambat, Jérôme Knebelmann, Bertrand Nobili, François Novo, Robert Podracka, Ludmila Roussey-Kesler, Gwenaëlle Granier, Luc-André Pediatr Nephrol Original Article BACKGROUND: A new prolonged-release formulation of potassium citrate and potassium bicarbonate, ADV7103, has been shown to improve metabolic control, palatability, and gastrointestinal safety in patients with distal renal tubular acidosis (dRTA) when compared to standard of care (SoC) treatments. The present work evaluates safety and efficacy of ADV7103 during 24 months. METHODS: Thirty pediatric and adult patients were included in an open-label extension study after a phase II/III trial. Safety and tolerability were assessed. Plasma bicarbonate and potassium levels, as well as urine parameters, were evaluated over time. Acceptability, adherence, and quality of life were also assessed. The evolution of clinical consequences of dRTA in the cohort was explored. RESULTS: There were 104 adverse events (AEs) reported, but only 9 gastrointestinal events observed in five patients (17%) were considered to be related to ADV7103 treatment. There were no AEs leading to treatment discontinuation. Plasma bicarbonate and potassium levels were in the normal ranges at the different visits, respectively, in 69–86% and 83–93% of patients. Overall adherence rates were ≥ 75% throughout the whole study in 79% patients. An average improvement of quality of life of 89% was reported at 24 months of study. CONCLUSIONS: Common AEs concerned metabolism and gastrointestinal disorders; the former being related to the disease. Less than half of the gastrointestinal AEs were related to ADV7103 treatment and they were mostly mild in severity. Metabolic parameters were maintained in the normal ranges in most patients. Patient satisfaction was high and adherence to treatment was good and remained stable. TRIAL REGISTRATION NUMBER: Registered as EudraCT 2013-003828-36 on the 3rd of September 2013. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00467-020-04873-0. Springer Berlin Heidelberg 2021-02-26 2021 /pmc/articles/PMC8172410/ /pubmed/33635379 http://dx.doi.org/10.1007/s00467-020-04873-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Bertholet-Thomas, Aurélia Guittet, Catherine Manso-Silván, Maria A. Joukoff, Sophie Navas-Serrano, Victor Baudouin, Véronique Cailliez, Mathilde Di Maio, Massimo Gillion-Boyer, Olivia Golubovic, Emilija Harambat, Jérôme Knebelmann, Bertrand Nobili, François Novo, Robert Podracka, Ludmila Roussey-Kesler, Gwenaëlle Granier, Luc-André Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis |
title | Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis |
title_full | Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis |
title_fullStr | Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis |
title_full_unstemmed | Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis |
title_short | Safety, efficacy, and acceptability of ADV7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis |
title_sort | safety, efficacy, and acceptability of adv7103 during 24 months of treatment: an open-label study in pediatric and adult patients with distal renal tubular acidosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8172410/ https://www.ncbi.nlm.nih.gov/pubmed/33635379 http://dx.doi.org/10.1007/s00467-020-04873-0 |
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