Literature DB >> 31235532

TransCon CNP, a Sustained-Release C-Type Natriuretic Peptide Prodrug, a Potentially Safe and Efficacious New Therapeutic Modality for the Treatment of Comorbidities Associated with Fibroblast Growth Factor Receptor 3-Related Skeletal Dysplasias.

Vibeke Miller Breinholt1, Caroline E Rasmussen2, Per Holse Mygind2, Mads Kjelgaard-Hansen2, Frank Faltinger2, Ana Bernhard2, Joachim Zettler2, Ulrich Hersel2.   

Abstract

TransCon CNP is a C-type natriuretic peptide (CNP-38) conjugated via a cleavable linker to a polyethylene glycol carrier molecule, designed to provide sustained systemic CNP levels upon weekly subcutaneous administration. TransCon CNP is in clinical development for the treatment of comorbidities associated with achondroplasia. In both mice and cynomolgus monkeys, sustained exposure to CNP via TransCon CNP was more efficacious in stimulating bone growth than intermittent CNP exposure. TransCon CNP was well tolerated with no adverse cardiovascular effects observed at exposure levels exceeding the expected clinical therapeutic exposure. At equivalent dose levels, reductions in blood pressure and/or an increase in heart rate were seen following single subcutaneous injections of the unconjugated CNP-38 molecule or a daily CNP-39 molecule (same amino acid sequence as Vosoritide, USAN:INN). The half-life of the daily CNP-39 molecule in cynomolgus monkey was estimated to be 20 minutes, compared with 90 hours for CNP-38, released from TransCon CNP. C max for the CNP-39 molecule (20 µg/kg) was approximately 100-fold higher, compared with the peak CNP level associated with administration of 100 µg/kg CNP as TransCon CNP. Furthermore, CNP exposure for the daily CNP-39 molecule was only evident for up to 2 hours postdose (lower limit of quantification 37 pmol/l), whereas TransCon CNP gave rise to systemic exposure to CNP-38 for at least 7 days postdose. The prolonged CNP exposure and associated hemodynamically safe peak serum concentrations associated with TransCon CNP administration are suggested to improve efficacy, compared with short-lived CNP molecules, due to better therapeutic drug coverage and decreased risk of hypotension. SIGNIFICANCE STATEMENT: The hormone C-type natriuretic peptide (CNP) is in clinical development for the treatment of comorbidities associated with achondroplasia, the most common form of human dwarfism. The TransCon Technology was used to design TransCon CNP, a prodrug that slowly releases active CNP in the body over several days. Preclinical data show great promise for TransCon CNP to be an effective and well-tolerated drug that provides sustained levels of CNP in a convenient once-weekly dose, while avoiding high systemic CNP bolus concentrations that can induce cardiovascular side effects.
Copyright © 2019 by The American Society for Pharmacology and Experimental Therapeutics.

Entities:  

Year:  2019        PMID: 31235532     DOI: 10.1124/jpet.119.258251

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  11 in total

1.  A long-acting C-natriuretic peptide for achondroplasia.

Authors:  Eric L Schneider; Christopher W Carreras; Ralph Reid; Gary W Ashley; Daniel V Santi
Journal:  Proc Natl Acad Sci U S A       Date:  2022-07-18       Impact factor: 12.779

Review 2.  Molecular Mechanism of Induction of Bone Growth by the C-Type Natriuretic Peptide.

Authors:  Estera Rintz; Grzegorz Węgrzyn; Toshihito Fujii; Shunji Tomatsu
Journal:  Int J Mol Sci       Date:  2022-05-25       Impact factor: 6.208

3.  Natriuretic Peptide Expression and Function in GH3 Somatolactotropes and Feline Somatotrope Pituitary Tumours.

Authors:  Samantha M Mirczuk; Christopher J Scudder; Jordan E Read; Victoria J Crossley; Jacob T Regan; Karen M Richardson; Bigboy Simbi; Craig A McArdle; David B Church; Joseph Fenn; Patrick J Kenny; Holger A Volk; Caroline P Wheeler-Jones; Márta Korbonits; Stijn J Niessen; Imelda M McGonnell; Robert C Fowkes
Journal:  Int J Mol Sci       Date:  2021-01-22       Impact factor: 5.923

4.  In vitro and in vivo characterization of Recifercept, a soluble fibroblast growth factor receptor 3, as treatment for achondroplasia.

Authors:  Diogo Gonçalves; Guylène Rignol; Pierre Dellugat; Guido Hartmann; Stephanie Sarrazy Garcia; Jeffrey Stavenhagen; Luca Santarelli; Elvire Gouze; Christian Czech
Journal:  PLoS One       Date:  2020-12-28       Impact factor: 3.240

5.  The CNP/NPR-B/cGMP Axis is a Therapeutic Target in Calcific Aortic Stenosis.

Authors:  David W J Armstrong; Deepak K Gupta; Brian R Lindman; W David Merryman
Journal:  JACC Basic Transl Sci       Date:  2021-12-27

Review 6.  2021 FDA TIDES (Peptides and Oligonucleotides) Harvest.

Authors:  Danah Al Shaer; Othman Al Musaimi; Fernando Albericio; Beatriz G de la Torre
Journal:  Pharmaceuticals (Basel)       Date:  2022-02-13

Review 7.  Natriuretic Peptide-Based Novel Therapeutics: Long Journeys of Drug Developments Optimized for Disease States.

Authors:  Tomoko Ichiki; Atsushi Jinno; Yoshihisa Tsuji
Journal:  Biology (Basel)       Date:  2022-06-03

8.  Birth prevalence of achondroplasia: A systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Femke van Kessel; Rosa van Hoorn; Judith van den Bosch; Renée Shediac; Sarah Landis
Journal:  Am J Med Genet A       Date:  2020-08-17       Impact factor: 2.802

9.  Assessing physical symptoms, daily functioning, and well-being in children with achondroplasia.

Authors:  Kathryn M Pfeiffer; Meryl Brod; Alden Smith; Jill Gianettoni; Dorthe Viuff; Sho Ota; R Will Charlton
Journal:  Am J Med Genet A       Date:  2020-10-20       Impact factor: 2.802

Review 10.  Advantages and Disadvantages of Different Treatment Methods in Achondroplasia: A Review.

Authors:  Wiktoria Wrobel; Emilia Pach; Iwona Ben-Skowronek
Journal:  Int J Mol Sci       Date:  2021-05-25       Impact factor: 5.923

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