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Terminated Phase 3 Interventional Results available

Study of Relacorilant in Combination With Nab-Paclitaxel in Patients With Metastatic Pancreatic Ductal Adenocarcinoma

ClinicalTrials.gov ID: NCT04329949

Public ClinicalTrials.gov record NCT04329949. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 9:59 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Study of Relacorilant in Combination With Nab-Paclitaxel in Patients With Metastatic Pancreatic Ductal Adenocarcinoma (RELIANT)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 3, open-label study to evaluate the objective response rate (ORR), in patients with metastatic pancreatic ductal adenocarcinoma (mPDAC) treated with relacorilant in combination with nab-paclitaxel, according to blinded independent central review.

Study identification

NCT ID
NCT04329949
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Corcept Therapeutics
Industry
Enrollment
43 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2020 (Actual)
Primary completion
Aug 23, 2021 (Actual)
Completion
Mar 25, 2022 (Actual)
Last update posted
Nov 18, 2023

2020 – 2022

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Site #038 Scottsdale Arizona 85258 —
Site #171 Duarte California 91010 —
Site #076 Los Angeles California 90095 —
Site #032 Aurora Colorado 80045 —
Site #009 Atlanta Georgia 30322 —
Site #184 Goshen Indiana 46526 —
Site #065 Baltimore Maryland 21231 —
Site #058 Detroit Michigan 48201 —
Site #185 Omaha Nebraska 68114 —
Site #182 Buffalo New York 14263 —
Site #044 New York New York 10016 —
Site #222 New York New York 10016 —
Site #077 Columbus Ohio 43210 —
Site #186 Toledo Ohio 43614 —
Site #172 Pittsburgh Pennsylvania 15232 —
Site #175 Knoxville Tennessee 37920 —
Site #176 Nashville Tennessee 37232 —
Site #173 Seattle Washington 98195 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04329949, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 18, 2023 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04329949 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →