A Once-Weekly C-Type Natriuretic Peptide for Treatment of Heart Failure with Preserved Ejection Fraction

C-type natriuretic peptide (CNP) has therapeutic potential in heart failure with preserved ejection fraction (HFpEF) due to its broad range of beneficial effects on cardiovascular structure and function. This study presents the design of a CNP analogue (<b>65</b>) for once-weekly subcutaneous administration. The design of <b>65</b> incorporated five strategic substitutions and an engineered fatty acid protractor to enhance the chemical stability, improve the pharmacokinetics, and lower the isoelectric point (pI). Low pI was found to be essential for minimizing injection site reactions and improving subcutaneous bioavailability. <b>65</b> demonstrated a promising pharmacokinetic profile for once-weekly treatment and an improved bioavailability compared to high pI CNP analogs. Furthermore, <b>65</b> was engineered for solubility at pH 6.5 to enable stability in liquid formulation. <i>In vivo</i> assessments supported the therapeutic potential in HFpEF of fatty acid-derivatized low pI CNP analogues. <b>65</b> is currently under clinical investigation in Phase 1.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2025-12-11
DOI
https://doi.org/10.1021/acs.jmedchem.5c02467
Primary Topic
Heart Failure Treatment and Management
Type
article
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article

A Once-Weekly C-Type Natriuretic Peptide for Treatment of Heart Failure with Preserved Ejection Fraction

Gustav Røder, T. Pedersen, Lene Alifrangis, Henrik Rahbek-Nielsen et al.
Journal of Medicinal Chemistry
Heart Failure Treatment and Management
article

A Once-Weekly C-Type Natriuretic Peptide for Treatment of Heart Failure with Preserved Ejection Fraction

Gustav Røder, T. Pedersen, Lene Alifrangis, Henrik Rahbek-Nielsen, Charlotte M. Dalsgaard, Marika Ejby Reinau, Ken Coppieters, Christian Poulsen, Svend Poulsen, Jonas Wilbs, Rie Kristine Schjeltved, Trine Pagh Ludvigsen, Samual Charles Burnage, Anne Louise Bank Kodal, Lene Kongsgaard Nielsen, Simone Fulle, Steen Sørensen, Kim Sonne, Mette V. Østergaard, K. Madsen, Ulrike Leurs, Christian W. Tornøe, Rikke Kaae Kirk, Conor C. G. Scully, Pernille Gry Wulff-Larsen, Michael Nyberg, Mathilde Frederikke Bjørn Bonde, Hassan Jumaa, Kilian W. Conde‐Frieboes, Jeppe Kirchhoff, Albrecht Gruhler, Karen‐Margrethe Pedersen, Steffen Schmidt, Heidi S. Schultz, L Martis, Peter Madsen, Jonathan A. Ewald, Nina Nørager, Mette Friis Ottosen
article en

Abstract

C-type natriuretic peptide (CNP) has therapeutic potential in heart failure with preserved ejection fraction (HFpEF) due to its broad range of beneficial effects on cardiovascular structure and function. This study presents the design of a CNP analogue (<b>65</b>) for once-weekly subcutaneous administration. The design of <b>65</b> incorporated five strategic substitutions and an engineered fatty acid protractor to enhance the chemical stability, improve the pharmacokinetics, and lower the isoelectric point (pI). Low pI was found to be essential for minimizing injection site reactions and improving subcutaneous bioavailability. <b>65</b> demonstrated a promising pharmacokinetic profile for once-weekly treatment and an improved bioavailability compared to high pI CNP analogs. Furthermore, <b>65</b> was engineered for solubility at pH 6.5 to enable stability in liquid formulation. <i>In vivo</i> assessments supported the therapeutic potential in HFpEF of fatty acid-derivatized low pI CNP analogues. <b>65</b> is currently under clinical investigation in Phase 1.

Journal of Medicinal ChemistryVol. 68(24)
Novo Nordisk (Denmark) (DK)
Openalex Percentile: Top 43%
Heart Failure Treatment and Management
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