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On-Demand Virtual Symposium

The Evolving Landscape of Transthyretin Amyloidosis Cardiomyopathy: New Therapies and Treatment Strategies

Release Date

May 6, 2025

Expiration Date

May 7, 2026

Credits

1.5 On-Demand

Topics

Cardiology, Rare Diseases

This activity was originally presented live at Asembia's AXS25 Summit in Las Vegas, Nevada on April 28, 2025.

Program Description
Transthyretin amyloidosis (ATTR) is a disorder caused by the misfolding of transthyretin (TTR) proteins, leading to fibril deposits in organs and tissues, with cardiac, neurologic, or mixed phenotypes. This session will focus specifically on transthyretin amyloid cardiomyopathy (ATTR-CM), exploring its unique pathophysiology, characterized by the deposition of misfolded TTR proteins in cardiac tissue, and the differentiation of ATTR-CM from other forms of ATTR. Delays in recognizing ATTR-CM and initiating appropriate management can exacerbate symptoms, reduce quality of life, and increase unnecessary health care resource utilization. Advances in research have introduced disease-modifying therapies (DMTs) specifically for ATTR-CM, which can slow disease progression and improve survival. This session will examine current and emerging treatment strategies with a focus on recent clinical trial data and evolving management guidelines. Faculty will utilize case-based discussion to explore practical considerations for treatment selection, therapy monitoring, and addressing challenges in patient care. Pharmacists will gain actionable insights to support the multidisciplinary management of ATTR-CM, optimize therapy use, and improve outcomes for affected patients.

Target Audience: Managed care and specialty pharmacists

Type of Activity: Application
Release date: May 6, 2025
Expiration date: May 6, 2026
Learner level: Intermediate
Time to complete activity:
1.5 hours
Fee: Free

Educational Objectives

At the completion of this activity, participants will be able to:

  • Identify the disease burden of transthyretin amyloidosis cardiomyopathy (ATTR-CM), considering factors such as health care utilization, misdiagnosis, and quality of life for patients
  • Examine clinical recommendations for treatment of ATTR-CM, taking into account the mechanisms of action, administration, dosing, and potential adverse effects of current and emerging therapies
  • Use clinical evidence for approved and investigational therapies for ATTR-CM in the development of patient-specific treatment plans
  • Manage the impact of high health care utilization in ATTR-CM through strategies to optimize multidisciplinary interventions and patient access to therapy
The Evolving Landscape of Transthyretin Amyloidosis Cardiomyopathy: New Therapies and Treatment Strategies

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This activity is supported by educational grants from BridgeBio and Alnylam.

What's Included
  • Access your activities anytime, anywhere, with a computer, tablet or smartphone
  • Free access with a PTCE account
  • Pharmacy education designed to improve patient care

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The Evolving Landscape of Transthyretin Amyloidosis Cardiomyopathy: New Therapies and Treatment Strategies

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