Transthyretin amyloid cardiomyopathy (ATTR-CM) is a treatable disease, yet patients often experience delayed diagnosis and access to the most appropriate treatment.
Prof. Teresa Trenkwalder joined us live at ESC 2026 to record a short video sharing her highlights from three Alnylam symposia exploring the importance of earlier recognition of ATTR-CM and the impact of emerging therapies.
Watch Prof. Trenkwalder's video and view a selection of the slides from the symposia presentations to examine the latest clinical evidence that may influence future treatment strategies for patients with ATTR-CM.
Clinical takeaways
- ATTR-CM remains frequently misdiagnosed despite improved disease recognition and increased use of background therapy, highlighting a persistent unmet need in contemporary patients
- RNA interference (RNAi) therapeutics address the root cause of ATTR-CM by targeting transthyretin at its source
- Vutrisiran treatment demonstrated consistent clinical benefits in patients with ATTR-CM and is considered a first-line treatment option in ATTR-CM
2 MIN
Jun 2026
Downloadable
