Novel Relaxin Receptor RXFP1 Agonist AZD3427 in the Treatment of Heart Failure: A Phase 1a/b, First‐in‐Human, Randomized, Single‐Blind, Placebo‐Controlled Study

Author:

Connolly Kathleen1,George Richard2ORCID,Omar Sami3,Matsson Elin4,Åstrand Magnus4ORCID,Althage Magnus5,Pettersen Daniel6ORCID,Mohamed Esha7,Fang Kelly8ORCID,Lima Joao A. C.9ORCID,Kujacic Mirjana10,Ödesjö Helena10ORCID,Turton Michelle1,Johannesson Petra10,Gabrielsen Anders11ORCID,Ufnal Marcin12ORCID

Affiliation:

1. Early Clinical Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D AstraZeneca Cambridge UK

2. Development, Research and Early Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D AstraZeneca Gaithersburg MD

3. Research and Early Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D AstraZeneca Cambridge UK

4. Clinical Pharmacology and Quantitative Pharmacology, Clinical Pharmacology & Safety Sciences, BioPharmaceuticals R&D AstraZeneca Gothenburg Sweden

5. Translational Science and Experimental Medicine, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D AstraZeneca Gothenburg Sweden

6. Research and Early Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D AstraZeneca Gothenburg Sweden

7. Early Biometrics, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D AstraZeneca Gothenburg Sweden

8. Early Biometrics, Cardiovascular, Renal, and Metabolism, BioPharmaceuticals R&D AstraZeneca Gaithersburg MD

9. Cardiology Division, Department of Medicine Johns Hopkins Hospital Baltimore MD

10. Global Patient Safety, BioPharmaceuticals R&D AstraZeneca Gothenburg Sweden

11. Early Clinical Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D AstraZeneca Gothenburg Sweden

12. Early Clinical Development, Cardiovascular, Renal and Metabolism, BioPharmaceuticals R&D AstraZeneca Warsaw Poland

Abstract

Background Heart failure mortality remains high despite recent progress in pharmacological treatment. AZD3427 is a selective long‐acting analog of relaxin, a vasodilatory hormone with antifibrotic effects. We assessed the safety, pharmacokinetics, and pharmacodynamics of AZD3427 in healthy volunteers and patients with heart failure on standard‐of‐care therapy. Methods and Results In this first‐in‐human, phase 1a/b, randomized, single‐blind, placebo‐controlled study, healthy volunteers were randomized 6:2 to receive a single dose of AZD3427 or placebo by subcutaneous injection in 5 mixed‐ethnicity cohorts (5, 10, 30, 90, or 270 mg) and 1 Japanese‐descent cohort (270 mg), or by intravenous injection in 1 cohort (15 mg). After confirming safety and tolerability in healthy volunteers, 3 cohorts of patients with heart failure and left ventricular ejection fraction ≤40% and 3 cohorts with ejection fraction ≥41% were randomized 6:2 to receive 5 weekly doses of AZD3427 (5, 15, or 45 mg) or placebo by subcutaneous injection. In total, 56 healthy volunteers and 48 patients with heart failure were randomized. AZD3427 was well tolerated at all doses. After subcutaneous administration, AZD3427 was absorbed slowly, and exposure was approximately linear across the dose range. In patients with heart failure, AZD3427 terminal half‐life was 13 to 14 days and there were numerical increases in stroke volume and estimated glomerular filtration rate. No treatment‐emergent antidrug antibodies were detected. Conclusions AZD3427 had favorable safety and pharmacokinetic profiles. Hemodynamic changes in patients with heart failure were consistent with the anticipated effects of a relaxin analog. These findings support further development of AZD3427 as a novel long‐term treatment for patients with heart failure. Registration URL: https://www.clinicaltrials.gov ; Unique Identifier: NCT04630067.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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