Testosterone cypionate is a synthetic derivative of testosterone in the form of an oil-soluble 17 (beta)-cyclopentylpropionate ester. Its benefit compared to other testosterone derivatives is the slow rate of release after injection and longer half-life. It was developed by the company Pharmacia and Upjohn and FDA approved on July 25, 1979.
Testosterone cypionate is used in males that present conditions derived from a deficiency or absence of endogenous testosterone. These conditions are 1) primary hypogonadism, defined as the testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome or orchidectomy; and 2) hypogonadotropic hypogonadism characterized by idiopathic gonadotropin, LHRH deficiency or pituitary-hypothalamic injury from tumors, trauma or radiation.
Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States
Roswell Park Cancer Institute, Buffalo, New York, United States
Brigham and Women's Hospital, Boston, Massachusetts, United States
Yale Cancer Center, New Haven, Connecticut, United States
Johns Hopkins University: Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States
Fred Hutch/University of Washington Cancer Consortium, Seattle, Washington, United States
Brigham and Women's Hospital, Boston, Massachusetts, United States
IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain
Emory University Hospital/Winship Cancer Institute, Atlanta, Georgia, United States
CTTB - Centro de Tratamento de Tumores Botafogo (Oncoclínicas), Rio De Janeiro, Brazil
HMV - Hospital Moinhos de Vento, Porto Alegre, Rio Grande Do Sul, Brazil
Hospital Sírio-Libanês SP, São Paulo, Brazil
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