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Study identifier: NCT07213297 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Comprehensive Program for Hereditary Transthyretin Amyloidosis

Condition: Amyloidosis in Transthyretin (TTR) · Amyloidosis, Familial  ·  Sponsor: Hospital de Alta Complejidad en Red

PhaseN/A
Planned participants20
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The Comprehensive Program for Hereditary Transthyretin Amyloidosis describes a prospective observational study focused on understanding hereditary transthyretin amyloidosis (ATTR), a progressive and potentially fatal condition marked by amyloid fibril deposits impacting multiple organs. The trial aims to characterize patient phenotypes, investigate factors affecting disease progression, and identify minimum criteria for disease onset. Conducted at Néstor Kirchner Hospital, the trial enrolls participants over 18 years old with confirmed pathogenic TTR variants. It includes thorough evaluations such as genetic testing sponsored by pharmaceutical companies, clinical assessments, and diverse diagnostic tests.

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

Talk to the study team

Gisela Zanga, MD  ·  +5491156074899  ·  gzanga84@hotmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Hospital Cuenca Alta de CañuelasCanuelas, Buenos Aires, ArgentinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07213297