Corcept Therapeutics Incorporated · NASDAQ:CORT

Corcept Therapeutics — SGO Annual Meeting on Women's Cancer 2026

18 slides from Corcept Therapeutics's conference presentation, Apr 10, 2026

  1. Slide 1: SGO Annual Meeting, San Juan, PR, April 10-13, 2026

    SAN JUAN, PR | APRIL 10-13, 2026 | WWW.SGO.ORG

  2. Slide 2: Financial Disclosure

    Financial Disclosure for: SAN JUAN, PR APRIL 10-13, 2026 Dr. Alexander B. Olawaiye I have the following financial relationships with ACCME defined ineligible companies to report over the past 24 months: AstraZeneca, Foundation Medicine, GSK, Merck, Daiichi Sankyo, Eisai, Corcept, and Eli Lilly Prese

  3. Slide 3: Unlabeled/Investigational Uses

    Unlabeled/Investigational Uses SAN JUAN, PR APRIL 10-13, 2026 Relacorilant in combination with nab-paclitaxel is FDA-approved as a treatment option for patients with platinum-resistant ovarian cancer, who have received 1–3 prior lines of therapy, including bevacizumab. This presentation may include

  4. Slide 4: Final Overall Survival Results From the Phase 3 ROSELLA Trial

    Final Overall Survival Results From the Phase 3 SAN JUAN, PR ROSELLA Trial: Relacorilant Plus Nab-Paclitaxel APRIL 10-13, 2026 vs Nab-Paclitaxel Monotherapy in Patients With Platinum-Resistant Ovarian Cancer (GOG-3073, ENGOT-ov72, APGOT-Ov10, LACOG-0223, and ANZGOG-2221/2023) Alexander B Olawaiye,1

  5. Slide 5: Background: Relacorilant Mechanism of Action

    Relacorilant Mechanism of Action Background Relacorilant MOA Relacorilant Cortisol SAN JUAN, PR APRIL 10-13, 2026 • Patients with platinum-resistant ovarian cancer have an overall survival of ~1 year and need new Multiprotein Glucocorticoid treatments1 Complex Receptor • Ovarian cancers express the

  6. Slide 6: Relacorilant Oncology Development Timeline

    Relacorilant Oncology Development Timeline SAN JUAN, PR APRIL 10-13, 2026 Nab-paclitaxel is one of the most efficacious therapies in patients with platinum-resistant ovarian cancer;1-3 as it does not require steroid pretreatment, it is a rational partner for relacorilant May 2020 Mar 2021 Feb 2025 J

  7. Slide 7: ROSELLA Study Schema

    ROSELLA | Study Schema SAN JUAN, PR APRIL 10-13, 2026 * Relacorilant (150 mg PO) Nab-paclitaxel (80 mg/m2 IV) Population DAY 1 8 15 28 Dual Primary Endpoints ▪ Epithelial ovarian, primary ▪ Progression-free survival (PFS) by peritoneal, or fallopian tube RECIST v1.1 per blinded cancer N=381 Relacori

  8. Slide 8: Baseline Characteristics Were Well Balanced

    ROSELLA | Baseline Characteristics Were Well Balanced Relacorilant + Nab-paclitaxel (N=188) Nab-paclitaxel (N=193) Age, median (range), years 61 (26–85) 62 (33–86) SAN JUAN, PR APRIL 10-13, 2026 White 136 (72.3) 135 (69.9) Black or African-American 3 (1.6) 2 (1.0) Race, n (%) Asian (92% Korean) 22 (

  9. Slide 9: Relacorilant Significantly Improved Progression-Free Survival

    ROSELLA | Relacorilant Significantly Improved Progression-Free Survival Assessed by Blinded Review at the Primary Analysis SAN JUAN, PR APRIL 10-13, 2026 Relacorilant + Nab-paclitaxel Nab-paclitaxel N=193 N=188 Events, n (%) 113 (60.1) 121 (62.7) 6m PFS Median PFS, m 6.5 (5.6–7.4) 5.5 (3.9–5.9) (95%

  10. Slide 10: Relacorilant Significantly Improved Overall Survival at Final Analysis

    ROSELLA | Relacorilant Significantly Improved Overall Survival at the Final Analysis SAN JUAN, PR Relacorilant + APRIL 10-13, 2026 Nab-paclitaxel Nab-paclitaxel N=193 N=188 Events, n (%) 129 (69%) 159 (82%) Median OS, m 16.0 (13.0–18.3) 11.9 (10.0–13.8) (95% CI) HR (95% CI) 0.65 (0.51–0.83) P-value

  11. Slide 11: Relacorilant Improved Overall Survival Across Key Subgroups

    ROSELLA | Relacorilant Improved Overall Survival Across Key Subgroups Subgroup Patients, n Events, n Hazard Ratio (95% CI) All Patients 381 288 0.65 (0.51–0.83) SAN JUAN, PR APRIL 10-13, 2026 <65 years 229 172 0.75 (0.55–1.01) Age ≥65 years 152 116 0.58 (0.39–0.85) North America 90 71 0.47 (0.28–0.7

  12. Slide 12: First and All Subsequent Therapies Were Well Balanced

    ROSELLA | First and All Subsequent Therapies Were Well Balanced First Subsequent Anticancer Therapies* SAN JUAN, PR APRIL 10-13, 2026 100% 2 1 0 1 1 1 All Subsequent Systemic Anticancer Therapies 90% 1 11 1 10 2 1 Relacorilant + Nab-paclitaxel 80% Nab-paclitaxel Monotherapy Percentage of Participant

  13. Slide 13: Safety Summary

    ROSELLA | Safety Summary Relacorilant + Nab-paclitaxel was Well-Tolerated, with a Favorable and Consistent Safety Profile SAN JUAN, PR APRIL 10-13, 2026 Safety Population Who Received at Least Relacorilant + Nab-paclitaxel Nab-paclitaxel One Dose of Study Drug (N=378) (N=188) (N=190) Weeks of nab-pa

  14. Slide 14: Treatment Discontinuations Due to Adverse Events Were Infrequent

    ROSELLA | Treatment Discontinuations Due to Adverse Events Were Infrequent SAN JUAN, PR APRIL 10-13, 2026 Kaplan-Meier Curve Showing Time to First Onset of Adverse Events Leading to Treatment Discontinuation Relacorilant + Nab-paclitaxel Nab-paclitaxel N=190 N=188 Events, n (%) 18 (9.6%) 15 (7.9%) H

  15. Slide 15: Common (>20%) Adverse Events

    ROSELLA | Common (>20%) Adverse Events SAN JUAN, PR APRIL 10-13, 2026 When adjusted for duration of exposure, the incidence rates of neutropenia and anemia were similar between study arms. Peripheral neuropathy occurred with similar frequency in both arms (19.1% and 17.4%). 5 SAEs of febrile neutrop

  16. Slide 16: Conclusions

    ROSELLA | Conclusions SAN JUAN, PR APRIL 10-13, 2026 At the primary analysis, the addition of relacorilant (a first-in-class SGRA) to nab-paclitaxel resulted ROSELLA met both in a statistically and clinically significant improvement in PFS by BICR (HR 0.70, P=0.0076). dual primary 1 At the final ana

  17. Slide 17: Acknowledgements

    ROSELLA | Acknowledgements Thank you to all the patients, caregivers, family members, investigators, and site staff who supported this global trial. SAN JUAN, PR APRIL 10-13, 2026 Alvarez Jewell Barlow Cho Churruca Galaz Aguil Guerrero Agyemang-Prempeh Bellier Azzouquoa Knowles Clamp Kim de la Cueva

  18. Slide 18: Access Full Manuscript

    Access Full manuscript Copies of this presentation obtained through QR code are for personal use only and may not be reproduced without written permission of the authors. Scan to access Presentation

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