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Adverse Event Reporting Information

Submit a Medical Inquiry

To report a medical adverse event, side effect, or product complaint, please call 1-855-844-3270.
Mon-Fri 8am – 8pm ET

You may also contact the U.S. Food and Drug Administration
MedWatch Adverse Event Reporting program:
Online: www.fda.gov/medwatch
Telephone: 1-800-FDA-1088

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Therapeutic Area

2022

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Adverse Event Reporting Information

2022

Poster

Phase 2 Results of Relacorilant + Nab-Paclitaxel in Patients with Recurrent, Platinum-resistant Ovarian Cancer with and Without Prior Bevacizumab

International Gynecologic Cancer Society (IGCS) Annual Global Meeting

2022

Presentation

Glucocorticoid Receptor Expression and Activity in a Phase 2 Ovarian Cancer Trial of the Glucocorticoid Receptor Modulator Relacorilant in Combination with Nab-Paclitaxel

European Society for Medical Oncology (ESMO) Congress

2022

Poster

Phase 1 Results of Exicorilant + Enzalutamide in Patients with Castration-Resistant Prostate Cancer

European Society for Medical Oncology (ESMO) Congress

2022

Poster

Relacorilant + Nab-paclitaxel in Patients with Recurrent, Platinum-resistant Ovarian Cancer: Phase 2 Subgroup Analysis Mirroring the Patient Population of an Upcoming Phase 3 Study

European Society for Medical Oncology (ESMO) Congress

2022

Presentation

Overall survival data from a 3-arm randomized phase 2 study of relacorilant, a selective glucocorticoid receptor modulator, combined with nab-paclitaxel in patients with recurrent platinum-resistant ovarian cancer

American Society of Clinical Oncology (ASCO) Annual Meeting

2022

Poster

A study of relacorilant in combination with nab-paclitaxel in metastatic pancreatic ductal adenocarcinoma (mPDAC)

American Society of Clinical Oncology (ASCO) Annual Meeting

2022

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To report a medical adverse event, side effect, or product complaint, please call 1-855-844-3270.
Mon-Fri 8am – 8pm ET

You may also contact the U.S. Food and Drug Administration MedWatch Adverse Event Reporting program:
Online: www.fda.gov/medwatch
Telephone: 1-800-FDA-1088

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