Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Abiraterone acetate + methylprednisolone is a combination therapy used primarily for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and metastatic high-risk castration-sensitive prostate cancer (CSPC). Abiraterone acetate is a prodrug of abiraterone, which acts as a selective and irreversible inhibitor of the enzyme steroid 17-hydroxylase/17,20 lyase (CYP17A1), thereby blocking androgen biosynthesis that fuels prostate cancer growth. Methylprednisolone, a synthetic glucocorticoid corticosteroid, is co-administered to mitigate mineralocorticoid-related side effects such as hypertension, hypokalemia, and fluid retention caused by CYP17A1 inhibition. The combination improves survival in patients with advanced prostate cancer who have progressed despite androgen deprivation therapy[2][3][5][8].
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 abiraterone acetate + methylprednisolone.