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LETTER |
The author is the Journals associate editor for HIV/AIDS and lesbian-gay-bisexual-transgender health.
Correspondence: Requests for reprints should be sent to Michael Gross, PhD, 1601 18th St NW, #716, Washington DC 20009 (e-mail: m144@earthlink.net).
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In the June 2003 issue of the Journal, I posed the rhetorical question of why clinical trials of "pre-exposure prophylaxis" against sexual transmission were being planned for populations in developing countries, but not for men who have sex with men (MSM) who are at high risk of contracting HIV in the United States.1 As that issue of the Journal was in press, the Centers for Disease Control and Prevention (CDC) published plans to support a randomized, placebo-controlled trial of the extended safety and preliminary efficacy of once-daily oral administration of the antiretroviral drug tenofovir disoproxil fumarate (Viread) among high-risk MSM.2
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