Review
International Journal of Impotence Research (2007) 19, 2–24. doi:10.1038/sj.ijir.3901366; published online 29 September 2005
Testosterone replacement therapy for male hypogonadism: Part III. Pharmacologic and clinical profiles, monitoring, safety issues, and potential future agents
A Seftel1
1Department of Urology, Case Western Reserve University, University Hospitals of Cleveland, Cleveland, OH, USA
Correspondence: Dr A Seftel, Department of Urology, Case Western Reserve University, 11100 Euclid Avenue, Cleveland, OH 44106-5046, USA. E-mail: adseftel@aol.com
Received 2 March 2005; Accepted 7 June 2005; Published online 29 September 2005.
Abstract
Male hypogonadism is associated with potentially distressing adverse effects on diverse organs and tissues. These include sexual dysfunction, particularly diminished libido, as well as mood disturbances, reduced lean body mass, and increased adipose-tissue mass. A wide range of effective and well-tolerated options exists. These include relatively noninvasive therapies, such as testosterone (T) gels and T patches; slightly more invasive treatments, such as the T buccal system; and invasive therapies, such as intramuscular T injections and subcutaneous depot implants (T pellets). Testosterone replacement therapy (TRT) can be individualized to enhance patient health and well-being. Screening and ongoing monitoring are necessary to ensure both the efficacy and safety of TRT, particularly prostate safety. Investigational agents, including selective androgen receptor modulators, may offer new pharmacodynamic and/or pharmacokinetic properties that enhance outcomes of TRT.
Keywords:
efficacy, hypogonadism, pharmacokinetics, safety, testosterone, tolerability
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