Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Intrinsa is a transdermal testosterone patch designed to deliver 300 mcg of testosterone per day. It was developed by Warner Chilcott and Procter & Gamble specifically for the treatment of hypoactive sexual desire disorder (HSDD) in postmenopausal women, particularly those who have undergone bilateral oophorectomy and hysterectomy (surgical menopause) and are receiving concomitant estrogen therapy. The patch works by restoring testosterone levels to a physiological range, thereby targeting androgen receptors in the brain and peripheral tissues to improve sexual desire and reduce associated distress. While it received marketing authorization in the European Union in 2006 for surgically menopausal women, the FDA issued a "not approvable" letter in 2004 due to concerns regarding long-term cardiovascular and breast cancer safety. The product was eventually withdrawn from the European market by the manufacturer in 2012 for commercial reasons.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on Intrinsa.