Relacorilant With Nab-Paclitaxel and Gemcitabine in Patients With Metastatic Pancreatic Adenocarcinoma

Inclusion Criteria:

• Signed and dated informed consent form prior to screening procedures

• Histologic diagnosis or cytologic diagnosis of pancreatic adenocarcinoma (PDAC)

• Initial diagnosis of metastatic disease occurred ≤6 weeks prior to enrollment in thestudy

• Life expectancy of ≥3 months

• Radiographic confirmation of metastatic disease with at least 1 distant tumormetastasis measurable on radiology imaging per RECIST version 1.1 criteria

• Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1

• Able to provide informed consent and comply with protocol requirements

• Able to swallow and retain oral medication and does not have uncontrolled emesis

• Has adequate gastrointestinal absorption

• Received no prior systemic anticancer therapy to treat metastatic disease

• If a patient received prior treatment of PDAC with chemotherapy, disease progressionmust have occurred >12 months after completing the last dose, and no persistenttreatment-related toxicities can be present.

• Adequate organ function

• Negative pregnancy test for patients of childbearing potential

• Agree to use protocol defined precautions to avoid pregnancy

Exclusion Criteria:

• Any major surgery within 4 weeks prior to enrollment

• Prior treatment as follows:

1. Radiotherapy, surgery, chemotherapy, immunotherapy, investigational therapy forthe treatment of metastatic disease

2. Systemic, inhaled, or prescription strength topical corticosteroids within 5times the half-life of the corticosteroid used prior to first dose of studydrug

• Received gemcitabine or nab-paclitaxel to treat their PDAC

• Known germline or somatic breast cancer gene (BRCA) mutation

• Peripheral neuropathy from any cause >Grade 1

• Medical conditions requiring chronic or frequent treatment with corticosteroids

• History of severe hypersensitivity or severe reaction to any of study drugs or theirexcipients

• Concurrent treatment with mifepristone or other glucocorticoid receptor modulators.

• Uncontrolled condition(s) which, may confound the results of the trial or interferewith the patient's safety or participation

• Active infection with HIV, hepatitis C or hepatitis B virus

• Known untreated parenchymal brain metastasis or uncontrolled central nervous systemmetastases

• History of other malignancy within 3 years prior to enrollment

• Taking protocol-prohibited medications

• Concurrent treatment with other investigational treatment studies for cancer

• Has received a live vaccine within 30 days prior to the study start date