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Study identifier: NCT07338942 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Implementation of Standardized Early Identification and Diagnosis for Transthyretin Amyloidosis (ATTR) in High-Risk Populations

Condition: ATTR-CM  ·  Sponsor: AstraZeneca

PhaseNA
Planned participants4000
Who can joinAll sexes, 60 Years to no upper limit
Healthy volunteersNo

About this study

This multicenter, prospective, single-arm, interventional study will enroll about 4,000 adult patients at high risk of ATTR amyloidosis from around 50 sites in China. Eligible patients are aged ≥60 years and have documented symptomatic heart failure with left ventricular ejection fraction ≥40% and LVH. Exclusion criteria include known etiologies of myocardial diseases, anomalies of serum free light chain or serum immunofixation electrophoresis, acute myocardial infarction within 6 months before screening, and inability to undergo 99mTc-PYP. Patients will undergo a 14-week diagnostic process. The study intervention involves knowledge training, operation training and post-training verification among investigators. Knowledge training for CV department investigators will cover disease-specific knowledge, standard diagnostic pathways, and genetics; training for investigators in echocardiology (ECHO) and nuclear medicine departments will focus on disease knowledge, standardized operating procedures (SOPs), and imaging parameter reporting. Operation training includes hands-on training in SOPs and image interpretation for ECHO and nuclear medicine investigators. Post-training verification will assess site-level compliance. Extra training will be arranged if quality audit is off target. The primary endpoint is the proportion of patients diagnosed with ATTR amyloidosis in high-risk populations. Secondary endpoints include the proportion of patients with ATTRwt amyloidosis, concordanc…

This description comes directly from the study's public registry record.

Talk to the study team

AstraZeneca Clinical Study Information Center  ·  1-877-240-9479  ·  information.center@astrazeneca.com

Always discuss trial participation with your own doctor first.

Locations (48)

Research SiteBeijing, ChinaNot Yet Recruiting
Research SiteBeijing, ChinaNot Yet Recruiting
Research SiteBeijing, ChinaNot Yet Recruiting
Research SiteBeijing, ChinaNot Yet Recruiting
Research SiteBeijing, ChinaNot Yet Recruiting
Research SiteChanglexi, ChinaNot Yet Recruiting
Research SiteChangsha, ChinaNot Yet Recruiting
Research SiteChangsha, ChinaNot Yet Recruiting
Research SiteChangsha, ChinaNot Yet Recruiting
Research SiteChengdu, ChinaNot Yet Recruiting
Research SiteChengdu, ChinaNot Yet Recruiting
Research SiteChongqing, ChinaNot Yet Recruiting

+ 36 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07338942