4.7 Article

Development of a long-acting relaxin analogue, LY3540378, for treatment of chronic heart failure

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 180, Issue 15, Pages 1965-1980

Publisher

WILEY
DOI: 10.1111/bph.16055

Keywords

long-acting; pharmacodynamics; pharmacokinetics; relaxin

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Chronic heart failure, especially in heart failure with preserved ejection fraction, lacks effective treatment options and poses a burden on patients and society. LY3540378, a long-acting relaxin analogue, has shown promising results in preclinical studies and is progressing in clinical trials, offering a potential therapeutic approach for chronic heart failure.
Background and PurposeChronic heart failure, a progressive disease with limited treatment options currently available, especially in heart failure with preserved ejection fraction (HFpEF), represents an unmet medical need as well as an economic burden. The development of a novel therapeutic to slow or reverse disease progression would be highly impactful to patients and society. Relaxin-2 (relaxin) is a human hormone regulating cardiovascular, renal, and pulmonary adaptations during pregnancy. A short-acting recombinant relaxin, Serelaxin, demonstrated short-term heart failure symptom relief and biomarker improvement in acute heart failure trials. Here, we present the development of a long-acting relaxin analogue to be tested in the treatment of chronic heart failure. Experimental ApproachLY3540378 is a long-acting protein therapeutic composed of a human relaxin analogue and a serum albumin-binding VHH domain. Key ResultsLY3540378 is a potent agonist of the relaxin family peptide receptor 1 (RXFP1) and maintains selectivity against RXFP2/3/4 comparable to native relaxin. The half-life of LY3540378 in preclinical species is extended through high affinity binding of the albumin-binding VHH domain to serum albumin. When tested in a single dose administration, LY3540378 elicited relaxin-mediated pharmacodynamic responses, such as reduced serum osmolality and increased renal blood flow in rats. In an isoproterenol-induced cardiac hypertrophy mouse model, treatment with LY3540378 significantly reduced cardiac hypertrophy and improved isovolumetric relaxation time. In a monkey cardiovascular safety study, there were no adverse observations from administration of LY3540378. Conclusion and ImplicationsLY3540378 demonstrated to be a suitable clinical development candidate, and is progressing in clinical trials.

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