Drug maker urges group to lobby FDA on testosterone for women

BMJ 2004; 329 doi: 10.1136/bmj.329.7477.1255 (Published 25 November 2004)
Cite this as: BMJ 2004;329:1255.1

Access to the full text of this article requires a subscription or payment. Please log in or subscribe below.

  1. Ray Moynihan
  1. Washington, DC

    The major household products manufacturer Procter & Gamble recently sought support from an international medical society, which it sponsors, asking the group to get involved in a regulatory hearing assessing the company's experimental testosterone patch.

    No peer reviewed data on the testosterone patch have been published, but it has been granted a fast track review by the US Food and Drug Administration and will be publicly debated by an advisory panel next week. The patch is the first drug to be assessed for a controversial condition called hypoactive sexual desire disorder.

    Procter & Gamble wrote to the International Society for the Study of Women's Sexual Health, whose recent conference it sponsored, urging the society to “participate” in next week's meeting …

    Access to the full text of this article requires a subscription or payment

    Article access

    Article access for 1 day

    Purchase this article for £20 $30 €32*

    The PDF version can be downloaded as your personal record

    * Prices do not include VAT

    THIS WEEK'S POLL