Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lybrel is a continuous-use oral contraceptive formulation containing a combination of the synthetic progestogen levonorgestrel (90 mcg) and the estrogen ethinyl estradiol (20 mcg). Developed by Wyeth (now a wholly owned subsidiary of Pfizer), it was the first combination oral contraceptive approved for daily administration 365 days a year, effectively eliminating the hormone-free interval and the associated withdrawal bleeding. The drug's primary mechanism of action involves the suppression of gonadotropins (follicle-stimulating hormone and luteinizing hormone), which inhibits ovulation. Additionally, it induces changes in the cervical mucus to increase viscosity and impede sperm transport, and alters the endometrium to reduce the likelihood of implantation. Lybrel was approved by the FDA on May 22, 2007, but was later discontinued from the market due to low commercial usage.
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 Lybrel.