Hypertrophic Cardiomyopathy Research and Drug Development Services
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* Please note that all of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.

Hypertrophic Cardiomyopathy Research and Drug Development Services

Inquiry

Hypertrophic cardiomyopathy refers to an increase in cardiac weight and volume that occurs in response to multiple injurious factors to accommodate an increase in the work done by the heart. Ace Therapeutics aims to provide integrated services for basic research and drug development for hypertrophic cardiomyopathy, so as to further investigate the pathogenesis of hypertrophic cardiomyopathy as well as therapeutic approaches.


Overview of Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy is a common inherited primary cardiomyopathy caused mainly by pathogenic mutations in the genes encoding myocardial sarcomere-associated proteins. Hypertrophic cardiomyopathy presents as a progressive damaging lesion of cardiomyocytes and is clinically characterized by thickening of the ventricular wall. It is now generally accepted that most hypertrophic cardiomyopathy is a monogenic disorder, triggered primarily by variants in the genes encoding myocardial sarcomere-associated proteins.

Fig. 1 Therapeutic strategies for obstructive hypertrophic cardiomyopathy.Fig. 1 Therapeutic strategies for obstructive hypertrophic cardiomyopathy. (Braunwald E, et al., 2023)

Current Status of Drug Development for Hypertrophic Cardiomyopathy

In 2016, the introduction of Mavacamten, a small molecule inhibitor of myocardial ganglionic contractile proteins, marked the beginning of the development of therapeutic drugs specific for hypertrophic cardiomyopathy. Recently, a growing number of drugs have been developed for different types and targets of hypertrophic cardiomyopathy.

Overview of Novel Drug Development for Hypertrophic Cardiomyopathy

Drug Name Drug Target Original Organization Drug Phase
Mavacamten Cardiac myosin Bristol Myers Squibb Co. Approved
Metoprolol Tartrate β1-adrenergic receptor AstraZeneca PLC Approved
Aficamten Cardiac myosin Cytokinetics, Inc. Phase 3
Tc-99m-annexin V-128 Phosphatidylserine Advanced Accelerator Applications USA, Inc. Phase 2
DiNA-001 MYBPC3 DiNAQOR AG Phase 1
TN-201 MYBPC3 Tenaya Therapeutics, Inc. Phase 1
What We Can Do

Ace Therapeutics is committed to supporting basic research and development of novel therapeutic approaches for hypertrophic cardiomyopathy by providing outsourced research services for disease model development and research technology platforms.

Research Models

Research Models

Basic Research

Basic Research

Drug Development

Drug Development

Research Models for Hypertrophic Cardiomyopathy


A suitable research model is essential for hypertrophic cardiomyopathy research. We are committed to providing diversified development services for animal models of hypertrophic cardiomyopathy to help our clients advance basic research and drug discovery in hypertrophic cardiomyopathy.

Custom Animal Models of Hypertrophic Cardiomyopathy

Based on customers' individual experimental needs, we can build a variety of hypertrophic cardiomyopathy models through different modeling methods, which include surgical narrowing of the aorta, drug or chemical induced hypertrophic cardiomyopathy models.

Transgenic Animal Model Development Services

We are able to provide customized transgenic or knockout animal models to support animal studies on the pathogenic mechanisms of hypertrophic cardiomyopathy, including but not limited to the following genes:

  • MYH7
  • MYL2
  • MYL3
  • MYBPC
  • TNNT2
  • TNNI3
  • TPM1
  • ACTC1

Genetically Engineered Mouse Models

We can provide the following high quality genetically engineered mice for hypertrophic cardiomyopathy.

Cardiomyocytes

For in vitro research, we are able to provide our customers with a wide range of cardiomyocyte cell lines.

  • Cardiomyocyte Cell Lines
  • hiPSC-CMs Development Services

Basic Research Services for Hypertrophic Cardiomyopathy


We aim to help our clients solve the difficulties encountered in the research of hypertrophic cardiomyopathy, and provide professional research services including novel biomarker development, pathology and imaging tests.

Novel Biomarker Discovery Services

It is important to detect biomarkers in the blood both to predict the development of hypertrophic cardiomyopathy and to aid in its diagnosis. Based on our professional multi-omics research technology platform, we are able to provide customized discovery and identification of novel biomarkers for hypertrophic cardiomyopathy.

  • Proteomic Profiling Services
  • Metabolomic Profiling Services

Pathology and Imaging Services

For animal research of hypertrophic cardiomyopathy, we can provide researchers with pathology and imaging services that enable intuitive model validation and efficacy assessment, including but not limited to:

  • Histopathology Services
  • Immunohistochemistry Services
  • Ultra-micro histological Study Services
  • In Vivo Optical Imaging Services
  • Electrocardiography Examination Services
  • Echocardiogram Examination Services
  • Computed Tomography Services
  • Magnetic Resonance Imaging Services
  • Radionuclide Imaging Services

Drug Development Services for Hypertrophic Cardiomyopathy


We can provide research and development services for hypertrophic cardiomyopathy drug therapies, including but not limited to the following drug types and targets:

R&D Services by Drug Type

R&D Services by Target

  • Cardiac Myosin
  • β1-adrenergic Receptor
  • Natriuretic Peptide Receptor A (NPRA)
  • C-Type Natriuretic Peptide Receptor (NPRC)
  • Myosin Binding Protein C3 (MYBPC3)
  • Calcium Channel

Ace Therapeutics has accumulated extensive knowledge in the field of hypertrophic cardiomyopathy, which can provide our customers with basic research, biomarker development, and novel therapies discovery services. If you are interested in our research services for hypertrophic cardiomyopathy, please do not hesitate to contact us.

Reference
  1. Braunwald, E.; et al. Mavacamten: a first-in-class myosin inhibitor for obstructive hypertrophic cardiomyopathy. Eur Heart J. 2023, 44(44): 4622-4633.
! All of our services and products are intended for preclinical research use only and cannot be intended for any clinical use.
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