Relacorilant (glucocorticoid receptor antagonist) + nab-paclitaxel extends OS by 4.1 months in platinum-resistant ovarian cancer
- Trial ID
- NCT05257408 on ClinicalTrials.gov
- Cancer type
- Ovarian, Fallopian, or Primary Peritoneal Cancer
- Published in
- New in Oncology - June 25, 2026
Relacorilant is a first-in-class, selective glucocorticoid receptor (GR) antagonist intended to counter GR-mediated chemotherapy resistance, and was combined with weekly nab-paclitaxel in the Phase 3 ROSELLA trial (GOG-3073; NCT05257408) in platinum-resistant ovarian cancer (n=381) versus nab-paclitaxel alone (dose-reduced in the combo arm: 80 mg/m² vs 100 mg/m²). At final OS analysis (288 deaths; 76% maturity; median follow-up 24.8 months), the combination improved OS to 16.0 vs 11.9 months (HR 0.65, 95% CI 0.51–0.83; p=0.0004); as a benchmark, historical nab-paclitaxel monotherapy in platinum-resistant disease has shown ORR ~23% with median PFS ~4.5 months and OS ~17.4 months in a GOG Phase 2 dataset (cross-trial comparisons apply). Taxane pretreatment was essentially universal (99.5%), and the OS benefit was directionally consistent across “taxane-free interval” (≤6 months: HR 0.60; >6 months: HR 0.66) and whether a taxane was part of the most recent regimen (taxane last: HR 0.67; no taxane last: HR 0.63); safety was stated as similar to nab-paclitaxel alone, but Grade 3+ AE details were not provided in this abstract.
Take home
If the tolerability truly holds up with full AE reporting, a statistically significant 4.1-month OS gain on top of weekly taxane—still a workhorse in platinum-resistant ovarian cancer—would be a meaningful, practice-relevant advance, but the subgroup splits here are small and not powered, so the “prior taxane” story should stay descriptive rather than definitive.
Source: Read the original publication
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