Effects of danicamtiv, a novel cardiac myosin activator, in heart failure with reduced ejection fraction: experimental data and clinical results from a phase 2a trial.


Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
09 2020
Historique:
received: 27 05 2020
revised: 04 06 2020
accepted: 10 06 2020
pubmed: 20 6 2020
medline: 19 5 2021
entrez: 20 6 2020
Statut: ppublish

Résumé

Both left ventricular (LV) and left atrial (LA) dysfunction and remodelling contribute to adverse outcomes in heart failure with reduced ejection fraction (HFrEF). Danicamtiv is a novel, cardiac myosin activator that enhances cardiomyocyte contraction. We studied the effects of danicamtiv on LV and LA function in non-clinical studies (ex vivo: skinned muscle fibres and myofibrils; in vivo: dogs with heart failure) and in a randomized, double-blind, single- and multiple-dose phase 2a trial in patients with stable HFrEF (placebo, n = 10; danicamtiv, n = 30; 50-100 mg twice daily for 7 days). Danicamtiv increased ATPase activity and calcium sensitivity in LV and LA myofibrils/muscle fibres. In dogs with heart failure, danicamtiv improved LV stroke volume (+10.6 mL, P < 0.05) and LA emptying fraction (+10.7%, P < 0.05). In patients with HFrEF (mean age 60 years, 25% women, ischaemic heart disease 48%, mean LV ejection fraction 32%), treatment-emergent adverse events, mostly mild, were reported in 17 patients (57%) receiving danicamtiv and 4 patients (40%) receiving placebo. Danicamtiv (at plasma concentrations ≥2000 ng/mL) increased stroke volume (up to +7.8 mL, P < 0.01), improved global longitudinal (up to -1.0%, P < 0.05) and circumferential strain (up to -3.3%, P < 0.01), decreased LA minimal volume index (up to -2.4 mL/m Danicamtiv was well tolerated and improved LV systolic function in patients with HFrEF. A marked improvement in LA volume and function was also observed in patients with HFrEF, consistent with pre-clinical findings of direct activation of LA contractility.

Identifiants

pubmed: 32558989
doi: 10.1002/ejhf.1933
pmc: PMC7689751
doi:

Substances chimiques

Angiotensin Receptor Antagonists 0
Angiotensin-Converting Enzyme Inhibitors 0
Cardiac Myosins EC 3.6.1.-

Types de publication

Clinical Trial, Phase II Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1649-1658

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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Auteurs

Adriaan A Voors (AA)

University of Groningen, Groningen, The Netherlands.

Jean-François Tamby (JF)

MyoKardia, Brisbane, CA, USA.

John G Cleland (JG)

Robertson Centre for Biostatistics and Clinical Trials Unit, University of Glasgow, Glasgow, UK.

Michael Koren (M)

Jacksonville Center for Clinical Research, Jacksonville, FL, USA.

Leslie B Forgosh (LB)

HealthEast Heart Care, Saint Paul, MN, USA.

Dinesh Gupta (D)

Tennova Healthcare-Harton, Tullahoma, TN, USA.

Lars H Lund (LH)

Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital, Heart and Vascular Theme, Stockholm, Sweden.

Albert Camacho (A)

Oregon Health & Science University, Portland, OR, USA.

Ravi Karra (R)

Department of Medicine, Duke University Medical Center, Durham, NC, USA.

Henk P Swart (HP)

Antonius Ziekenhuis Sneek, Sneek, The Netherlands.

Pierpaolo Pellicori (P)

Robertson Centre for Biostatistics and Clinical Trials Unit, University of Glasgow, Glasgow, UK.

Frank Wagner (F)

Charité Research Organization, Berlin, Germany.

Ray E Hershberger (RE)

Divisions of Human Genetics and Cardiovascular Medicine, The Ohio State University, Columbus, OH, USA.

Narayana Prasad (N)

Cardiovascular Imaging Core Laboratory, Brigham and Women's Hospital, Boston, MA, USA.

Robert Anderson (R)

MyoKardia, Brisbane, CA, USA.

Anu Anto (A)

MyoKardia, Brisbane, CA, USA.

Kaylyn Bell (K)

MyoKardia, Brisbane, CA, USA.

Jay M Edelberg (JM)

MyoKardia, Brisbane, CA, USA.

Liang Fang (L)

MyoKardia, Brisbane, CA, USA.

Marcus Henze (M)

MyoKardia, Brisbane, CA, USA.

Cynthia Kelly (C)

MyoKardia, Brisbane, CA, USA.

Gregory Kurio (G)

MyoKardia, Brisbane, CA, USA.

Wanying Li (W)

MyoKardia, Brisbane, CA, USA.

Kate Wells (K)

MyoKardia, Brisbane, CA, USA.

Chun Yang (C)

MyoKardia, Brisbane, CA, USA.

Sam L Teichman (SL)

Teichman Drug Development Consulting, Oakland, CA, USA.

Carlos L Del Rio (CL)

MyoKardia, Brisbane, CA, USA.

Scott D Solomon (SD)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

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Classifications MeSH