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The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD

RATIONALE & OBJECTIVE: Venglustat, a glucosylceramide synthase inhibitor, inhibits cyst growth and reduces kidney failure in mouse models of autosomal dominant polycystic kidney disease (ADPKD). STAGED-PKD aims to determine the safety and efficacy of venglustat and was designed using patient enr...

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Autores principales: Perrone, Ronald D., Hariri, Ali, Minini, Pascal, Ahn, Curie, Chapman, Arlene B., Horie, Shigeo, Knebelmann, Bertrand, Mrug, Michal, Ong, Albert C.M., Pei, York P.C., Torres, Vicente E., Modur, Vijay, Gansevoort, Ronald T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529969/
https://www.ncbi.nlm.nih.gov/pubmed/36204243
http://dx.doi.org/10.1016/j.xkme.2022.100538
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author Perrone, Ronald D.
Hariri, Ali
Minini, Pascal
Ahn, Curie
Chapman, Arlene B.
Horie, Shigeo
Knebelmann, Bertrand
Mrug, Michal
Ong, Albert C.M.
Pei, York P.C.
Torres, Vicente E.
Modur, Vijay
Gansevoort, Ronald T.
author_facet Perrone, Ronald D.
Hariri, Ali
Minini, Pascal
Ahn, Curie
Chapman, Arlene B.
Horie, Shigeo
Knebelmann, Bertrand
Mrug, Michal
Ong, Albert C.M.
Pei, York P.C.
Torres, Vicente E.
Modur, Vijay
Gansevoort, Ronald T.
author_sort Perrone, Ronald D.
collection PubMed
description RATIONALE & OBJECTIVE: Venglustat, a glucosylceramide synthase inhibitor, inhibits cyst growth and reduces kidney failure in mouse models of autosomal dominant polycystic kidney disease (ADPKD). STAGED-PKD aims to determine the safety and efficacy of venglustat and was designed using patient enrichment for progression to end-stage kidney disease and modeling from prior ADPKD trials. STUDY DESIGN: STAGED-PKD is a 2-stage, international, double-blind, randomized, placebo-controlled trial in adults with ADPKD (Mayo Class 1C-1E) and estimated glomerular filtration rate (eGFR) 45-<90 mL/min/1.73 m(2) at risk of rapidly progressive disease. Enrichment for rapidly progressing patients was identified based on retrospective analysis of total kidney volume (TKV) and eGFR slope from the combined Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease and HALT Progression of Polycystic Kidney Disease A studies. SETTING & PARTICIPANTS: Target enrollment in stages 1 and 2 was 240 and 320 patients, respectively. INTERVENTIONS: Stage 1 randomizes patients 1:1:1 to venglustat 8 mg or 15 mg once daily or placebo. Stage 2 randomizes patients 1:1 to placebo or venglustat, with the preferred dose based on stage 1 safety data. OUTCOMES: Primary endpoints are TKV growth rate over 18 months in stage 1 and eGFR slope over 24 months in stage 2. Secondary endpoints include: annualized rate of change in eGFR from baseline to 18 months (stage 1); annualized rate of change in TKV based on magnetic resonance imaging from baseline to 18 months (stage 2); and safety, tolerability, pain, and fatigue (stages 1 and 2). LIMITATIONS: If stage 1 is unsuccessful, patients enrolled in the trial may develop drug-related adverse events that can have long-lasting effects. CONCLUSIONS: Modeling allows the design and powering of a 2-stage combined study to assess venglustat’s impact on TKV growth and eGFR slope. Stage 1 TKV assessment via a nested approach allows early evaluation of efficacy and increased efficiency of the trial design by reducing patient numbers and trial duration. FUNDING: This study was funded by Sanofi. TRIAL REGISTRATION: STAGED-PKD has been registered at ClinicalTrials.gov with study number NCT03523728.
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spelling pubmed-95299692022-10-05 The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD Perrone, Ronald D. Hariri, Ali Minini, Pascal Ahn, Curie Chapman, Arlene B. Horie, Shigeo Knebelmann, Bertrand Mrug, Michal Ong, Albert C.M. Pei, York P.C. Torres, Vicente E. Modur, Vijay Gansevoort, Ronald T. Kidney Med Original Research RATIONALE & OBJECTIVE: Venglustat, a glucosylceramide synthase inhibitor, inhibits cyst growth and reduces kidney failure in mouse models of autosomal dominant polycystic kidney disease (ADPKD). STAGED-PKD aims to determine the safety and efficacy of venglustat and was designed using patient enrichment for progression to end-stage kidney disease and modeling from prior ADPKD trials. STUDY DESIGN: STAGED-PKD is a 2-stage, international, double-blind, randomized, placebo-controlled trial in adults with ADPKD (Mayo Class 1C-1E) and estimated glomerular filtration rate (eGFR) 45-<90 mL/min/1.73 m(2) at risk of rapidly progressive disease. Enrichment for rapidly progressing patients was identified based on retrospective analysis of total kidney volume (TKV) and eGFR slope from the combined Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease and HALT Progression of Polycystic Kidney Disease A studies. SETTING & PARTICIPANTS: Target enrollment in stages 1 and 2 was 240 and 320 patients, respectively. INTERVENTIONS: Stage 1 randomizes patients 1:1:1 to venglustat 8 mg or 15 mg once daily or placebo. Stage 2 randomizes patients 1:1 to placebo or venglustat, with the preferred dose based on stage 1 safety data. OUTCOMES: Primary endpoints are TKV growth rate over 18 months in stage 1 and eGFR slope over 24 months in stage 2. Secondary endpoints include: annualized rate of change in eGFR from baseline to 18 months (stage 1); annualized rate of change in TKV based on magnetic resonance imaging from baseline to 18 months (stage 2); and safety, tolerability, pain, and fatigue (stages 1 and 2). LIMITATIONS: If stage 1 is unsuccessful, patients enrolled in the trial may develop drug-related adverse events that can have long-lasting effects. CONCLUSIONS: Modeling allows the design and powering of a 2-stage combined study to assess venglustat’s impact on TKV growth and eGFR slope. Stage 1 TKV assessment via a nested approach allows early evaluation of efficacy and increased efficiency of the trial design by reducing patient numbers and trial duration. FUNDING: This study was funded by Sanofi. TRIAL REGISTRATION: STAGED-PKD has been registered at ClinicalTrials.gov with study number NCT03523728. Elsevier 2022-08-27 /pmc/articles/PMC9529969/ /pubmed/36204243 http://dx.doi.org/10.1016/j.xkme.2022.100538 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research
Perrone, Ronald D.
Hariri, Ali
Minini, Pascal
Ahn, Curie
Chapman, Arlene B.
Horie, Shigeo
Knebelmann, Bertrand
Mrug, Michal
Ong, Albert C.M.
Pei, York P.C.
Torres, Vicente E.
Modur, Vijay
Gansevoort, Ronald T.
The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD
title The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD
title_full The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD
title_fullStr The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD
title_full_unstemmed The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD
title_short The STAGED-PKD 2-Stage Adaptive Study With a Patient Enrichment Strategy and Treatment Effect Modeling for Improved Study Design Efficiency in Patients With ADPKD
title_sort staged-pkd 2-stage adaptive study with a patient enrichment strategy and treatment effect modeling for improved study design efficiency in patients with adpkd
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9529969/
https://www.ncbi.nlm.nih.gov/pubmed/36204243
http://dx.doi.org/10.1016/j.xkme.2022.100538
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