Trimetazidine did not provide cardiac support in wild-type ATTR-CM
Trimetazidine did not improve heart function or exercise capacity in patients with wild-type transthyretin cardiac amyloidosis.
Trimetazidine did not improve heart function or exercise capacity in patients with wild-type transthyretin cardiac amyloidosis.
If approved, vutrisiran would become the first U.S. treatment to treat both polyneuropathy and cardiomyopathy linked to ATTR.
Nine years of treatment with tafamidis prevented hospitalizations for heart failure in two patients with ATTR-CM.
The study results suggested that tafamidis may stabilize ATTR-CM progression rather than reverse its effects.
Nucresiran showed potential as a treatment for transthyretin amyloidosis cardiomyopathy (ATTR-CM), Alnylam Pharmaceuticals said.
The FDA says the drug is designed to reduce death and hospitalizations related to transthyretin cardiac amyloidosis (ATTR-CM).
Arginine helped stabilize TTR tetramers and prevented amyloid formation, showing its potential as a safe way to stave off ATTR-CM.
SGLT2is appeared to be safe for patients with ATTR-CM and may result in fewer hospitalizations and improved kidney function.
The study results highlighted the need to broaden diagnostic criteria for transthyretin amyloid cardiomyopathy, or ATTR-CM.