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.

Autosomal dominant polycystic kidney disease modeling study design total kidney volume venglustat

Journal

Kidney medicine
ISSN: 2590-0595
Titre abrégé: Kidney Med
Pays: United States
ID NLM: 101756300

Informations de publication

Date de publication:
Oct 2022
Historique:
entrez: 7 10 2022
pubmed: 8 10 2022
medline: 8 10 2022
Statut: epublish

Résumé

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. 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 Target enrollment in stages 1 and 2 was 240 and 320 patients, respectively. 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. 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). If stage 1 is unsuccessful, patients enrolled in the trial may develop drug-related adverse events that can have long-lasting effects. 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. This study was funded by Sanofi. STAGED-PKD has been registered at ClinicalTrials.gov with study number NCT03523728.

Identifiants

pubmed: 36204243
doi: 10.1016/j.xkme.2022.100538
pii: S2590-0595(22)00160-1
pmc: PMC9529969
doi:

Banques de données

ClinicalTrials.gov
['NCT03523728']

Types de publication

Journal Article

Langues

eng

Pagination

100538

Informations de copyright

© 2022 The Authors.

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Auteurs

Ronald D Perrone (RD)

Division of Nephrology, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts.

Ali Hariri (A)

Eloxx Pharmaceuticals, Watertown, Massachusetts.

Pascal Minini (P)

Sanofi, Chilly Mazarin, France.

Curie Ahn (C)

Department of Internal Medicine, Seoul National University, Seoul, Republic of Korea.

Arlene B Chapman (AB)

Department of Medicine, University of Chicago, Chicago, Illinois.

Shigeo Horie (S)

Department of Urology, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Bertrand Knebelmann (B)

Université de Paris, AP-HP, Service de Néphrologie, Hôpital Necker-Enfants Malades, Paris, France.

Michal Mrug (M)

Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama and Department of Veterans Affairs Medical Center, Birmingham, Alabama.

Albert C M Ong (ACM)

Academic Nephrology Unit, Department of Infection Immunity & Cardiovascular Disease, University of Sheffield Medical School, Sheffield, United Kingdom.

York P C Pei (YPC)

Division of Nephrology, University of Toronto, Toronto, Ontario, Canada.

Vicente E Torres (VE)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota.

Vijay Modur (V)

Eloxx Pharmaceuticals, Watertown, Massachusetts.

Ronald T Gansevoort (RT)

Department of Nephrology, University Medical Center Groningen, The Netherlands.

Classifications MeSH