Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

Phase II trial of the effects of Pill-Plus triple-hormone oral contraceptive vs oral contraceptives alone on the sexual arousability and vascular component of sexual arousal response in women

X
Trial Profile

Phase II trial of the effects of Pill-Plus triple-hormone oral contraceptive vs oral contraceptives alone on the sexual arousability and vascular component of sexual arousal response in women

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 02 Jul 2010

Price : $35 *
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Drospirenone/estradiol/prasterone (Primary) ; Estradiol/drospirenone
  • Indications Female sexual dysfunction
  • Focus Pharmacodynamics
  • Most Recent Events

    • 01 Jul 2010 Positive clinical results announced in a BioSante Pharmaceuticals media release. Additional data will be reported upon full publication of the study results.
    • 30 Jun 2007 New trial record.

You need to be a logged in or subscribed to view this content Request demo

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top