| Literature DB >> 29941213 |
Tomoko Ichiki1, Nina Dzhoyashvili1, John C Burnett2.
Abstract
Cenderitide is a novel designer natriuretic peptide (NP) composed of C-type natriuretic peptide (CNP) fused to the C-terminus of Dendroaspis natriuretic peptide (DNP). Cenderitide was engineered to co-activate the two NP receptors, particulate guanylyl cyclase (pGC)-A and pGC-B. The rationale for its design was to achieve the renal-enhancing and anti-fibrotic properties of dual receptor activation, but without clinically significant hypotension. Here, we review the biology of the NPs and the rationale for their use in heart failure. Most importantly, we present the key studies related to the discovery of Cenderitide. Finally, we review the key clinical studies that have advanced this first-in-class dual NP receptor activator for heart failure.Entities:
Keywords: Designer natriuretic peptide; Drug development; Heart failure; Natriuretic peptide; Receptors
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Year: 2018 PMID: 29941213 PMCID: PMC6277229 DOI: 10.1016/j.ijcard.2018.06.002
Source DB: PubMed Journal: Int J Cardiol ISSN: 0167-5273 Impact factor: 4.164