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ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria

BACKGROUND: Primary hyperoxalurias (PHs) are rare genetic diseases that increase the endogenous level of oxalate, a waste metabolite excreted predominantly by the kidneys and also the gut. Treatments aim to improve oxalate excretion, or reduce oxalate generation, to prevent kidney function deteriora...

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Autores principales: Ariceta, Gema, Collard, Laure, Abroug, Saoussen, Moochhala, Shabbir H., Gould, Edward, Boussetta, Abir, Ben Hmida, Mohamed, De, Sudarsana, Hunley, Tracy E., Jarraya, Faical, Fraga, Gloria, Banos, Ana, Lindner, Elisabeth, Dehmel, Bastian, Schalk, Gesa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763141/
https://www.ncbi.nlm.nih.gov/pubmed/35552824
http://dx.doi.org/10.1007/s00467-022-05591-5
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author Ariceta, Gema
Collard, Laure
Abroug, Saoussen
Moochhala, Shabbir H.
Gould, Edward
Boussetta, Abir
Ben Hmida, Mohamed
De, Sudarsana
Hunley, Tracy E.
Jarraya, Faical
Fraga, Gloria
Banos, Ana
Lindner, Elisabeth
Dehmel, Bastian
Schalk, Gesa
author_facet Ariceta, Gema
Collard, Laure
Abroug, Saoussen
Moochhala, Shabbir H.
Gould, Edward
Boussetta, Abir
Ben Hmida, Mohamed
De, Sudarsana
Hunley, Tracy E.
Jarraya, Faical
Fraga, Gloria
Banos, Ana
Lindner, Elisabeth
Dehmel, Bastian
Schalk, Gesa
author_sort Ariceta, Gema
collection PubMed
description BACKGROUND: Primary hyperoxalurias (PHs) are rare genetic diseases that increase the endogenous level of oxalate, a waste metabolite excreted predominantly by the kidneys and also the gut. Treatments aim to improve oxalate excretion, or reduce oxalate generation, to prevent kidney function deterioration. Oxalobacter formigenes is an oxalate metabolizing bacterium. This Phase III, double-blind, placebo-controlled randomized trial investigated the effectiveness of orally administered Oxabact™, a lyophilized O. formigenes formulation, at reducing plasma oxalate levels in patients suffering from PH. METHODS: Subjects (≥ 2 years of age) with a diagnosis of PH and maintained but suboptimal kidney function (mean estimated glomerular filtration rate at baseline < 90 mL/min/1.73 m(2)) were eligible to participate. Subjects were randomized to receive Oxabact or placebo twice daily for 52 weeks. Change from baseline in plasma oxalate concentration at Week 52 was the primary study endpoint. RESULTS: Forty-three subjects were screened, 25 were recruited and one was discontinued. At Week 52, O. formigenes was established in the gut of subjects receiving Oxabact. Despite decreasing plasma oxalate level in subjects treated with Oxabact, and stable/increased levels with placebo, there was no significant difference between groups in the primary outcome (Least Squares mean estimate of treatment difference was − 3.80 μmol/L; 95% CI: − 7.83, 0.23; p-value = 0.064). Kidney function remained stable in both treatments. CONCLUSIONS: Oxabact treatment may have stabilized/reduced plasma oxalate versus a rise with placebo, but the difference over 12 months was not statistically significant (p = 0.06). A subtle effect observed with Oxabact suggests that O. formigenes may aid in preventing kidney stones. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material including a graphical abstract available at 10.1007/s00467-022-05591-5.
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spelling pubmed-97631412022-12-21 ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria Ariceta, Gema Collard, Laure Abroug, Saoussen Moochhala, Shabbir H. Gould, Edward Boussetta, Abir Ben Hmida, Mohamed De, Sudarsana Hunley, Tracy E. Jarraya, Faical Fraga, Gloria Banos, Ana Lindner, Elisabeth Dehmel, Bastian Schalk, Gesa Pediatr Nephrol Original Article BACKGROUND: Primary hyperoxalurias (PHs) are rare genetic diseases that increase the endogenous level of oxalate, a waste metabolite excreted predominantly by the kidneys and also the gut. Treatments aim to improve oxalate excretion, or reduce oxalate generation, to prevent kidney function deterioration. Oxalobacter formigenes is an oxalate metabolizing bacterium. This Phase III, double-blind, placebo-controlled randomized trial investigated the effectiveness of orally administered Oxabact™, a lyophilized O. formigenes formulation, at reducing plasma oxalate levels in patients suffering from PH. METHODS: Subjects (≥ 2 years of age) with a diagnosis of PH and maintained but suboptimal kidney function (mean estimated glomerular filtration rate at baseline < 90 mL/min/1.73 m(2)) were eligible to participate. Subjects were randomized to receive Oxabact or placebo twice daily for 52 weeks. Change from baseline in plasma oxalate concentration at Week 52 was the primary study endpoint. RESULTS: Forty-three subjects were screened, 25 were recruited and one was discontinued. At Week 52, O. formigenes was established in the gut of subjects receiving Oxabact. Despite decreasing plasma oxalate level in subjects treated with Oxabact, and stable/increased levels with placebo, there was no significant difference between groups in the primary outcome (Least Squares mean estimate of treatment difference was − 3.80 μmol/L; 95% CI: − 7.83, 0.23; p-value = 0.064). Kidney function remained stable in both treatments. CONCLUSIONS: Oxabact treatment may have stabilized/reduced plasma oxalate versus a rise with placebo, but the difference over 12 months was not statistically significant (p = 0.06). A subtle effect observed with Oxabact suggests that O. formigenes may aid in preventing kidney stones. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material including a graphical abstract available at 10.1007/s00467-022-05591-5. Springer Berlin Heidelberg 2022-05-12 2023 /pmc/articles/PMC9763141/ /pubmed/35552824 http://dx.doi.org/10.1007/s00467-022-05591-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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
Ariceta, Gema
Collard, Laure
Abroug, Saoussen
Moochhala, Shabbir H.
Gould, Edward
Boussetta, Abir
Ben Hmida, Mohamed
De, Sudarsana
Hunley, Tracy E.
Jarraya, Faical
Fraga, Gloria
Banos, Ana
Lindner, Elisabeth
Dehmel, Bastian
Schalk, Gesa
ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria
title ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria
title_full ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria
title_fullStr ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria
title_full_unstemmed ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria
title_short ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria
title_sort ephex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of oxalobacter formigenes in patients with primary hyperoxaluria
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763141/
https://www.ncbi.nlm.nih.gov/pubmed/35552824
http://dx.doi.org/10.1007/s00467-022-05591-5
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