Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Prionelle is a combined oral contraceptive (COC) developed and marketed by CampusPharma, specifically for the Nordic markets. It is a fixed-dose combination product containing 150 micrograms of levonorgestrel (a second-generation progestogen) and 30 micrograms of ethinylestradiol (a synthetic estrogen). Prionelle works by suppressing the mid-cycle surge of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), thereby inhibiting ovulation. It additionally increases the viscosity of cervical mucus to prevent sperm penetration and alters the endometrial lining to discourage implantation. Within the Nordic clinical guidelines, Prionelle is often recommended as a first-line contraceptive choice because levonorgestrel-containing combinations are associated with a lower risk of venous thromboembolism (VTE) compared to those containing third- or fourth-generation progestogens.
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 Prionelle.