Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
EF190 is a fixed-dose combination (FDC) drug candidate developed by Eurofarma, currently in Phase III clinical development for the treatment of moderate acne vulgaris in women. The formulation consists of a new concentration of cyproterone acetate, a steroidal antiandrogen and progestogen, combined with a reduced dose of ethinylestradiol, a synthetic estrogen. Cyproterone acetate works by competitively inhibiting the androgen receptor, thereby reducing the effects of testosterone and dihydrotestosterone on the sebaceous glands, which decreases sebum production. Ethinylestradiol contributes to the anti-acne effect by suppressing the hypothalamic-pituitary-ovarian axis, leading to reduced ovarian androgen synthesis and an increase in sex hormone-binding globulin (SHBG) levels, which further lowers the concentration of free circulating androgens. This combination is intended to provide a therapeutic benefit for acne while potentially improving the safety profile through the use of a lower estrogen dose compared to traditional formulations.
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 EF190.