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SILENCE-TTR

Study of the Impact of Vutrisiran versus Transthyretin StabiLizers on Efficacy and Safety in a RaNdomized, Controlled Trial to Evaluate Patients with TransThyRetin Amyloid Cardiomyopathy - SILENCE-TTR

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1051250227
Enrollment
360
Registered
2026-02-17
Start date
2026-01-13
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Transthyretin cardiac amyloidosis Amyloidosis,Disease-modifying drug,Scintigraphy

Interventions

Patients with ATTR-CM will be randomly assigned to receive either a TTR silencer (vutrisiran) or a TTR stabilizer (tafamidis or acoramidis).

Sponsors

Kitai Takeshi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients aged 18 years or older at the time of obtaining consent 2) Patients diagnosed with ATTR-CM who meet the criteria for disease-modifying therapy in Japan 3) New York Heart Association (NYHA) functional class 1-3 4) CohortA) Newly diagnosed with ATTR-CM and not receiving treatment with tafamidis, acoramidis, or butyric acid CohortB) Those already diagnosed with ATTR-CM and receiving treatment with Tafamidis or Acoramidis 5) Patients for whom written consent has been obtained from the patient themselves or their authorized representative

Exclusion criteria

Exclusion criteria: 1) Diagnosis of light-chain (AL) amyloidosis 2) Diagnosis of hereditary ATTR-CM (variant TTR genotype) 3) Maintaining dialysis patients 4) Patients with hypersensitivity to either Tafamidis, Acolamis, or Butiriciran 5) Patients who are already participating in or plan to participate in other clinical trials during the study period 6) Patients deemed unsuitable for participation in this study by the principal investigator or co-investigator for other reasons

Design outcomes

Primary

MeasureTime frame
The percentage change from baseline in standardized uptake value SUV on myocardial scintigraphy 99mTc HMDP or 99mTc PYP SPECT CT at week 52 after treatment initiation

Secondary

MeasureTime frame
1.Incidence and time to first onset of cardiac amyloidosis related adverse events at 104w after treatment initiation 2.Percent and absolute changes from baseline in the following parameters at 52w and 104w after treatment initiation -Myocardial scintigraphy 99mTc HMDP or 99mTc PYP SPECT CT standardized uptake value SUV at 104w -Cardiac MRI parameters late gadolinium enhancement LGE extracellular volume ECV and native T1 and T2 -Echocardiographic parameters left ventricular mass index LVMi left atrial volume index LAVI apical sparing ratio left ventricular ejection fraction LVEF and left ventricular volumes -Biomarkers NT proBNP or BNP troponin T or I transthyretin TTR and thyroid function free T4 free T3 and TSH -6 minute walk distance 6MWD -Kansas City Cardiomyopathy Questionnaire Overall Summary Score KCCQ OS -Short Physical Performance Battery SPPB, Handgrip strength , Clinical Frailty Scale

Contacts

Public ContactNao Tokimatsu

National Cerebral and Cardiovascular Center

silence-ttr@ncvc.go.jp+81-6-6170-1070

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026