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Not yet recruitingNCT05974644Updated Aug 12, 2026

Southeastern ATTR Amyloidosis Consortium: SEATTRAC Family Registry

An observational study in Amyloidosis, Hereditary, sponsored by Virginia Commonwealth University. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-12.

Sponsored by Virginia Commonwealth University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
1,000
Ages
18 Years and older
Sex
All
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Study summary

The study design is a prospective registry including asymptomatic and symptomatic patients who carry a pathogenic TTR mutation. The study will enroll patients who meet the inclusion criteria and none of the exclusion criteria until 1000 patients are enrolled, at which point in time the study investigators will evaluate whether further patient accrual is meaningful.

Read the detailed description

Hereditary transthyretin amyloidosis (hATTR) is an autosomal dominant disorder caused by a pathogenic mutation of the transthyretin (TTR) gene. The mutated gene destabilizes the TTR tetramer causing it to dissociate, misfold and accumulate as insoluble extracellular amyloid fibrils. These fibrils then deposit in various organs and tissues leading to organ dysfunction and destruction. There are more than 130 known pathogenic mutations of the TTR gene leading to hATTR with predominantly neurologic or cardiac clinical manifestations.

The V142I mutation (historically reported as V122I prior to the opening 20-amino acid sequence being included to the position count) is the most prevalent mutation in the United States. This mutation is carried by 3-4% of the Black population with a founder variant originating in West Africa. It was brought to the Western Hemisphere during the Atlantic slave trade. The presence of the mutation has been associated with increased risk of heart failure, however with incomplete penetrance of an amyloid cardiomyopathy phenotype. With improved accessibility to genetic testing and noninvasive techniques with bone scintigraphy to diagnose TTR deposition in the heart, the identification of disease has dramatically increased. As a result, genetic counseling and cascade testing has identified a growing pool of asymptomatic, at-risk family members for whom counseling and surveillance is undefined.

There is a paucity of data for V142I carriers including poor understanding of disease penetrance, timing of disease onset as well as onset of extracardiac manifestations. Prior studies that sought to understand disease penetrance and early clinical predictors of phenotype presentation were limited due to geographic variation, historical under-recognition of the disease, poor enrollment of Black V142I patients into clinical studies and missing data due to retrospective study designs. For example, the often-cited THAOS (Transthyretin Amyloidosis Outcomes Survey) registry demonstrated enrollment limitations. Of the 740 total asymptomatic hATTR mutation carriers studied, only 10 asymptomatic subjects had the V142 mutation.

Better described neuropathic or mixed variants (i.e. T80A [formerly T60A] and V50M [formerly V30M] are often associated with easily detectable, clinically debilitating and rapidly progressing disease earlier in life. Conversely the V142I phenotype presents later in life primarily with a cardiomyopathy that may mimic hypertensive heart disease or heart failure with preserved ejection fraction. Oftentimes symptoms in the older V142I patient population are attributed to other comorbidities such as diabetes, hypertension or valve disease. This contributes to a delay in the diagnosis of hATTR diagnosis or a miss altogether. Identifying early clinical predictors of disease presentation may offer an opportunity for meaningful interruption of disease progression with newly available disease modifying therapies.

In this study, members of the Southeastern ATTR Amyloidosis Consortium (SEATTRAC) will enroll asymptomatic carriers of pathogenic TTR mutations and hATTR cardiac amyloidosis patients in a prospective registry. SEATTRAC members include high volume amyloidosis centers that are not only destination centers for amyloidosis care, but comprehensively serve their local and regional communities. We anticipate that such a registry will be the first to describe the clinical course of disease and outcomes for asymptomatic carriers of the V142I mutation, the hATTR variant that predominantly afflicts Black Americans.

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Conditions studied

  • Amyloidosis, Hereditary

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03

In context

Amyloidosis, Familial

24 studies on the registry are indexed under Amyloidosis, Familial; 11 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 65 across 12 observational studies indexed under Amyloidosis, Familial.

Browse Amyloidosis, Familial studies →

Lead sponsor

Virginia Commonwealth University is the lead sponsor of 641 studies on the registry; 82 are open to participants now.

Of its 88 completed or terminated interventional studies of FDA-regulated products, 62 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Any carriers of a pathogenic TTR mutation known to cause hATTR amyloidosis will be recruited to the registry.

Inclusion criteria

  • Over the age of 18 years
  • Carrier of a pathogenic hATTR mutation confirmed on whole blood gene testing or mass spectrometry
  • Willing to return for required follow-up visits

Exclusion criteria

Exclusion Criteria:

  • Patient having undergone heart transplantation or implantation of mechanical circulatory support
  • Patients unable to provide informed consent
  • Patients having undergone liver transplantation
  • Patients have evidence of light chain amyloidosis
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
1,000 participants (estimated)
Target follow-up
3 Years
Patient registry
Yes

Groups and cohorts

  • Asymptomatic carriers

    Other: Registry

  • Patients with cardiac hereditary transthyretin amyloidosis (hATTR)

    Other: Registry

Interventions

  • OtherRegistry

    The purpose of this registry is to collect and store health information from people who are carriers of the gene known to cause hereditary amyloidosis and those with a confirmed diagnosis of the disease.

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What researchers measure

Primary outcomes

  1. The predictors and incidence of amyloidosis

    For those enrolled as asymptomatic carriers, it will be assessed if they develop cardiac or extra cardiac amyloidosis

    Time frame: 15 years

  2. Mortality and/or need for heart transplant

    For those with cardiac hereditary transthyretin amyloidosis (hATTR), it will be assessed how many participants die due to disease or require a heart transplant

    Time frame: 10 years

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Study locations

1 site
  • Virginia Commonwealth University
    Richmond, Virginia 23298, United States
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References and documents

Individual participant data

Plan to share: Yes — Deidentified data will be provided to the other investigators as a limited data set if requested.

Supporting information: Study protocol

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05974644
Lead sponsor
Virginia Commonwealth University
Responsible party
Sponsor
First posted
Aug 3, 2023
Start date
Sep 2026 (estimated)
Primary completion
Dec 1, 2030 (estimated)
Completion
Dec 1, 2030 (estimated)
Last update
Aug 12, 2026

Study contacts

Keyur Shah, MD
Contact
keyur.shah@vcuhealth.org
804-828-4571
Sarah Paciulli, NP
Contact
sarah.paciulli@vcuhealth.org
804-828-4571
Keyur Shah, MD
principal investigator · Virginia Commonwealth University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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