Triethylenetatramine (TETA), also known as trientine, is a potent and selective copper (II)-selective chelator. It is a structural analog of linear polyamine compounds, spermidine and spermine. TETA was first developed in Germany in 1861 and its chelating properties were first recognized in 1925. Initially approved by the FDA in 1985 as a second-line treatment for Wilson's disease, TETA is currently indicated to treat adults with stable Wilson’s disease who are de-coppered and tolerant to penicillamine.
TETA has been investigated in clinical trials for the treatment of heart failure in patients with diabetes.
Triethylenetetramine is a copper chelator indicated for the treatment of adult patients with stable Wilson’s disease who are de-coppered and tolerant to penicillamine.
University Hospitals of Leicester NHS Foundation Trust, Leicester, United Kingdom
Liverpool Heart and Chester Hospital NHS Foundation Trust, Liverpool, United Kingdom
Royal Brompton and Harefield NHS Foundation Trust, London, United Kingdom
Stern Cardiovascular, Germantown, Tennessee, United States
UCLA School of Medicine, Torrance, California, United States
Innovative Research of West Florida, Inc., Clearwater, Florida, United States
Nucleo de Pesquisa e Desenvolvimento de Medicamentos - Universidade Federal do Ceará - Rodolfo Teófilo, Fortaleza, Brazil
DiSCOG Gastroenterology Unit, Padova, Italy
Centre National de Référence Wilson, Hôpital Lariboisière, Paris, France
Chang Gung Memorial Hospital, Linkou, Taoyuan City, Taiwan
Universitätsklinik Heidelberg, Heidelberg, Germany
Kings College Hospital, London, United Kingdom
San Paolo Hospital UOC, Milan, Italy
Universitätsklinik Heidelberg, Heidelberg, Germany
Univeristy of British Columbia/Vancouver Coastal Health Authority - Eye Care Center, Vancouver, British Columbia, Canada
Eye Care Centre - Vancouver Coastal Health, Vancouver, British Columbia, Canada
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
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