Clinical EfficacyPivotal trial data showed relacorilant plus chemotherapy significantly reduced risk of death versus chemotherapy alone while maintaining a comparable safety profile, supporting its potential as a meaningful new therapy in platinum‑resistant ovarian cancer.
Commercial Strength And ExclusivityKorlym sales continue to expand and management projects a multibillion‑dollar opportunity, while solid cash reserves plus patents and orphan‑drug designations offer financial runway and market protection during commercialization.
Regulatory OutlookNDA for relacorilant in platinum‑resistant ovarian cancer has a PDUFA date of July 11, 2026 and analysts assign a high probability of approval, which could enable a new commercial launch and revenue stream.