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March 4, 2026European Heart Journal Supplements0 citationsOpen Access

Current available treatment options targeting TTR tetramer stabilization

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DJD P Judge

Key Points

  • To evaluate available pharmacological options targeting TTR stabilization for transthyretin amyloidosis.
  • Reviewed existing literature on TTR stabilizers
  • Highlighted approved treatments: tafamidis and acoramidis
  • Discussed surrogate markers for TTR stabilization
  • Both tafamidis and acoramidis received international approval for ATTR-CM
  • No direct comparisons of efficacy exist between approved TTR stabilizers
  • In vitro studies suggest effective TTR stabilization is achievable through these medications.

Abstract

Abstract Transthyretin (TTR) stabilization is a well-established method for the treatment of transthyretin amyloidosis, particularly involving the associated diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM). Four different oral pharmacologic TTR stabilizers have been used or proposed for treatment of this condition: diflunisal, tafamidis, tolcapone, and acoramidis. Two of them (acoramidis and tafamidis) have received international approval for use in patients with ATTR-CM, based on double-blinded, placebo-controlled clinical trials. To date, there have not been any head-to-head studies comparing the efficacy of these approved TTR stabilizers. This article describes the background and data supporting the use of tafamidis and acoramidis in people with ATTR-CM, including reports of blinded in vitro comparison, and surrogate markers for TTR tetramer stabilization, such as serum transthyretin levels.

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Cite This Study

D P Judge (2026) studied this question.

synapsesocial.com/papers/69a7ccb2d48f933b5eed85d6https://doi.org/10.1093/eurheartjsupp/suag010
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