transthyretin amyloidosis

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Information
Disease name
transthyretin amyloidosis
Disease ID
DOID:0050638
Description
"An amyloidosis that is characterized by a loss of sensation in the extremities, cardiomyopathy, nephropathy, vitreous opacities, and CNS amyloidosis resulting from abnormal deposits of amyloid protein in the body's organs and tissues and has_material_basis_in autosomal dominant inheritance of mutations in the TTR gene." [url:http\://en.wikipedia.org/wiki/Transthyretin-related_hereditary_amyloidosis, url:http\://ghr.nlm.nih.gov/condition/transthyretin-amyloidosis, url:http\://www.ncbi.nlm.nih.gov/books/NBK1194/, url:http\://www.orpha.net/consor4.01/www/cgi-bin/OC_Exp.php?lng=EN&Expert=85451, url:http\://www.paramiloidose.com/en/paramiloidose.php?a=2&id=25, url:https\://www.ncbi.nlm.nih.gov/books/NBK1194/, url:https\://www.ncbi.nlm.nih.gov/pubmed/19372706]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
NCT ID Status Phase Summary Start date Completion date
NCT03759379 Active, not recruiting Phase 3 HELIOS-A: A Study of Vutrisiran (ALN-TTRSC02) in Patients With Hereditary Transthyretin Amyloidosis (hATTR Amyloidosis) February 14, 2019 October 2026
NCT03431896 Active, not recruiting Monitoring of Early Disease Progression in Hereditary Transthyretin Amyloidosis February 1, 2018 December 31, 2026
NCT00628745 Completed Transthyretin Amyloidosis Outcome Survey (THAOS) January 4, 2008 June 16, 2023
NCT02792790 Completed Carpal Tunnel Syndrome and Amyloid Cardiomyopathy March 2016 December 2, 2021
NCT03190577 Completed N/A Assessment of the Prevalence of TTR Amyloid Neuropathy in a Population of Patients With Neuropathy of Unknown Aetiology September 21, 2017 May 23, 2022
NCT01171859 Completed Phase 2 Safety, Efficacy and Pharmacokinetics of Doxycycline Plus Tauroursodeoxycholic Acid in Transthyretin Amyloidosis July 2010 October 2015
NCT03352089 Completed Positron Emission Tomography / Magnetic Resonance Imaging in Aortic Stenosis November 1, 2017 August 23, 2018
NCT03588468 Completed N/A Expanding the Biomarkers in Familial Amyloid Neuropathy: MRI and Motor Unit Estimation by Electrophysiological Study September 20, 2018 December 18, 2019
NCT03591757 Completed Early Phase 1 Short-term Effects of TOLCAPONE on Transthyretin Stability in Subjects With Leptomeningeal TTR Amyloidosis (ATTR) October 30, 2018 April 26, 2019
NCT03923920 Completed Screening for Systemic Amyloidosis Via the Ligamentum Flavum May 1, 2019 December 2, 2021
NCT05075798 Completed Study of Cerebral MRI Anomalies in Mutated Transthyretin Amyloidosis Patients October 25, 2021 May 31, 2022
NCT02016365 Completed Phase 2 Safety and Efficacy Study of Doxycycline/UrsoDeoxyCholicAcid on Disease Progression in ATTR Amyloidosis February 2012 December 2014
NCT03860935 Completed Phase 3 Efficacy and Safety of AG10 in Subjects With Transthyretin Amyloid Cardiomyopathy March 19, 2019 May 11, 2023
NCT03862807 Completed Phase 3 Patisiran in Patients With Hereditary Transthyretin-mediated Amyloidosis (hATTR Amyloidosis) Disease Progression Post-Liver Transplant March 27, 2019 October 20, 2020
NCT03886155 Completed Cardiac Amyloidosis Screening at Trigger Finger Release May 1, 2019 December 2, 2021
NCT04569903 Not yet recruiting N/A Evaluation of a Claims-based Algorithm for the Identification of Transthyretin-mediated Amyloidosis (ATTR) Amyloidosis in Medical Records April 2024 February 2026
NCT06345235 Recruiting New Biomarkers and Plasma Prothrombotic Potential in Cardiac Transthyretin Amyloidosis July 11, 2023 July 11, 2024
NCT03237494 Recruiting TRAMmoniTTR Study Genetic Screening of an At-risk Population for hATTR and Monitoring of TTR Positive Subjects July 20, 2017 April 30, 2025
NCT04276220 Recruiting N/A Prevalence of wtATTR-CM After Carpal Tunnel Release Surgery April 1, 2020 January 2026
NCT05635045 Recruiting Phase 2 Evuzamitide in PET/CT to Measure Potential Therapeutic Response in ATTR July 8, 2022 September 1, 2024
NCT05758493 Recruiting Phase 2 Characterizing Iodine-124 Evuzumitide (AT-01) in Systemic Amyloidosis January 10, 2023 July 10, 2024
NCT05814380 Recruiting The Regional Scintigraphic DPD Uptake in Cardiac Transthyretin Amyloidosis. May 4, 2020 March 1, 2024
NCT05873868 Recruiting Myocardial Effects in Patients With ATTRv With Polyneuropathy Treated With Patisiran or Vutrisiran April 12, 2024 July 2026
NCT06291805 Recruiting Phenotyping and Characterization of wtATTR-CM (TRACE 1) February 20, 2024 December 2025
NCT04899180 Recruiting Early Phase 1 Prevalence of Transthyretin Cardiac Amyloidosis in Clinically Significant Aortic Stenosis July 14, 2023 August 2024
NCT05023889 Recruiting Early Phase 1 Spectrum of Peripheral and Autonomic Neuropathies in Patients With aTTRwt Amyloidosis and Response to Patisiran Therapy August 3, 2022 December 2024
NCT05409833 Recruiting Systemic Transthyretin Amyloidosis: Carpal Tunnel Syndrome in a Portuguese Population June 1, 2020 June 1, 2025
NCT05577819 Recruiting N/A Prevalence and Prediction of ATTR in Ambulatory Patients With HFpEF October 2, 2020 December 31, 2024
NCT04611204 Terminated Transthyretin Cardiac Amyloidosis in Patients With Idiopathic Carpal Tunnel Syndrome Referred for Release Surgery October 1, 2020 February 23, 2023
NCT04563286 Unknown status Patient-Reported Outcome Measures in Wild-Type and Variant Cardiac Transthyretin Amyloidosis February 22, 2020 June 22, 2022
NCT04513600 Unknown status ATTR-Cardiomyopathy Stabilization Following Tafamidis Therapy August 1, 2020 August 1, 2023
NCT04963985 Unknown status Phase 4 The Effect of Tafamidis on Transthyretin Stabilization, Safety, Tolerability and Efficacy in Transthyretin Amyloid Polyneuropathy Patients June 1, 2021 June 1, 2023
NCT02713880 Withdrawn Biomarker for Transthyretin-Related Familial Amyloidotic Polyneuropathy (BioTRAP) August 20, 2018 December 1, 2019
Disase is a (Disease Ontology)
DOID:9120
Cross Reference ID (Disease Ontology)
GARD:656
Cross Reference ID (Disease Ontology)
ICD10CM:E85.82
Cross Reference ID (Disease Ontology)
MIM:105210
Cross Reference ID (Disease Ontology)
ORDO:85447
Exact Synonym (Disease Ontology)
Amyloidosis, hereditary, transthyretin-related
Exact Synonym (Disease Ontology)
ATTR amyloidosis
Exact Synonym (Disease Ontology)
ATTRm amyloidosis
Exact Synonym (Disease Ontology)
Corino de Andrade's disease
Exact Synonym (Disease Ontology)
familial amyloid polyneuropathy
Exact Synonym (Disease Ontology)
Familial transthyretin amyloidosis
Exact Synonym (Disease Ontology)
paramyloidosis
Exact Synonym (Disease Ontology)
transthyretin-related hereditary amyloidosis
Exact Synonym (Disease Ontology)
TTR amyloidosis