Transthyretin Amyloidosis Clinical Trials

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Comprehensive Program for Hereditary Transthyretin Amyloidosis

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Participants with a pathogenic variant of the TTR gene (Hereditary Amyloidosis)

Locations
Other Locations
Argentina
Hospital Cuenca Alta de Cañuelas
RECRUITING
Cañuelas
Contact Information
Primary
Gisela Zanga, MD
gzanga84@hotmail.com
+5491156074899
Time Frame
Start Date: 2025-11-01
Estimated Completion Date: 2028-12-01
Participants
Target number of participants: 20
Treatments
Participants over 18 years of age diagnosed with hereditary transthyretin amyloidosis
Participants with a pathogenic variant of the TTR gene confirmed by genetic testing, whether symptomatic and/or with suspected disease progression, as well as asymptomatic carriers of these variants, will be included. Individuals with wild-type TTR amyloidosis will be excluded .
Sponsors
Leads: Hospital de Alta Complejidad en Red

This content was sourced from clinicaltrials.gov