RecruitingPhase 2NCT07259317

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

A Phase 2, Single-Arm Trial of Relacorilant in Combination With Nab-Paclitaxel and Gemcitabine in Patients With Previously Untreated Metastatic Pancreatic Adenocarcinoma (TRIDENT)


Sponsor

Corcept Therapeutics

Enrollment

60 participants

Start Date

Jan 27, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This is a Phase 2, single-arm study to evaluate the safety and efficacy of relacorilant in combination with nab-paclitaxel and gemcitabine in patients with previously untreated metastatic pancreatic adenocarcinoma (PDAC).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing relacorilant — a drug that blocks the stress hormone cortisol — combined with standard chemotherapy (nab-paclitaxel and gemcitabine) as a first-line treatment for people with metastatic pancreatic cancer. **You may be eligible if...** - You have been recently diagnosed with metastatic pancreatic adenocarcinoma (within the past 6 weeks) - Your cancer is measurable on scans - You are in reasonably good physical condition - Your life expectancy is at least 3 months **You may NOT be eligible if...** - You have previously received chemotherapy for metastatic pancreatic cancer - You have serious liver, kidney, or heart problems - You are on certain medications that interact with study drugs - You have an active infection or other condition making chemotherapy unsafe Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRelacorilant 150 mg once daily (QD)

Relacorilant will be administered as capsules for oral dosing on the day before (excluding Cycle 1, Day -1), the day of, and the day after nab-paclitaxel and gemcitabine infusions.

DRUGNab-paclitaxel 100 mg/m^2

Nab-paclitaxel will be administered via intravenous (IV) infusion on Days 1, 8, and 15 of each 28-day cycle.

DRUGGemcitabine 1000 mg/m^2

Gemcitabine will be administered via intravenous (IV) infusion on Days 1, 8, and 15 of each 28-day cycle.


Locations(10)

Site 02

Scottsdale, Arizona, United States

Site 04

Los Angeles, California, United States

Site 06

Atlanta, Georgia, United States

Site 03

Grand Rapids, Michigan, United States

Site 10

East Brunswick, New Jersey, United States

Site 08

Albany, New York, United States

Site 05

Lake Success, New York, United States

Site 07

Shirley, New York, United States

Site 09

Nashville, Tennessee, United States

Site 01

San Antonio, Texas, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

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NCT07259317


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