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

Sponsor

Corcept Therapeutics (Industry)

Overall Status

Terminated

CT.gov ID

NCT04329949

Collaborator

(none)

Enrollment

Locations

Arm

20.8

Actual Duration (Months)

2.4

Patients Per Site

0.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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

Condition or Disease	Intervention/Treatment	Phase
Metastatic Pancreatic Ductal Adenocarcinoma	Drug: Relacorilant, 100 mg and 25 mg Drug: Nab paclitaxel	Phase 3

Detailed Description

Relacorilant is a small molecule antagonist of the glucocorticoid receptor (GR). The goals of this study are to evaluate the efficacy, safety, and pharmacokinetics (PK) of relacorilant in combination with nab-paclitaxel in the treatment of metastatic pancreatic ductal adenocarcinoma.

Eligible patients are those with metastatic pancreatic adenocarcinoma (mPDAC) who have received at least 2 prior lines of therapy for pancreatic ductal adenocarcinoma (PDAC) in any setting, including at least 1 prior gemcitabine-based therapy and at least 1 prior fluoropyrimidine-based therapy.

Patients will receive treatment until progressive disease (PD) (per RECIST v1.1) as determined by the Investigator, experiencing unmanageable toxicity, or until other treatment discontinuation criteria are met. All patients will be followed for documentation of disease progression and survival information (i.e., date and cause of death) and subsequent treatment.

Study Design

Study Type:

Interventional

Actual Enrollment :

43 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

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

Actual Study Start Date :

Jun 30, 2020

Actual Primary Completion Date :

Aug 23, 2021

Actual Study Completion Date :

Mar 25, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Relacorilant with nab-paclitaxel Patients will be treated with relacorilant, administered orally, once daily in combination with nab-paclitaxel on Days 1, 8, and 15 of each 28-day cycle.	Drug: Relacorilant, 100 mg and 25 mg Relacorilant is supplied as capsules for oral dosing. Other Names: CORT125134 Drug: Nab paclitaxel Nab-paclitaxel is administered as IV infusion over 30 minutes on Days 1, 8, and 15 of each 28-day cycle. Other Names: Abraxane

Arm

Intervention/Treatment

Experimental: Relacorilant with nab-paclitaxel

Patients will be treated with relacorilant, administered orally, once daily in combination with nab-paclitaxel on Days 1, 8, and 15 of each 28-day cycle.

Drug: Relacorilant, 100 mg and 25 mg

Relacorilant is supplied as capsules for oral dosing.

Other Names:

CORT125134

Drug: Nab paclitaxel

Nab-paclitaxel is administered as IV infusion over 30 minutes on Days 1, 8, and 15 of each 28-day cycle.

Other Names:

Abraxane

Outcome Measures

Primary Outcome Measures

Objective Response Rate (ORR) per Blinded Independent Central Review (BICR) [Enrollment through 24 months]
Percentage of patients with measurable disease at baseline who achieved confirmed complete response (CR) or partial response (PR) per Response Evaluation Criteria in Solid Tumors (RESIST) v1.1, according to a Blinded Independent Central Review (BICR).

Secondary Outcome Measures

Objective Response Rate (ORR) per Investigator Assessment [Enrollment through 24 months]
Percentage of patients with measurable disease at baseline who achieved confirmed complete response (CR), partial response (PR), stable disease (SD) or progressive disease (PD) per Response Evaluation Criteria in Solid Tumors (RESIST) v1.1, according to Investigator assessment.
Best Overall Response (BoR) [Enrollment through 24 months]
To evaluate the best overall response per RESIST v1.1.
Duration of Response (DoR) [Time of response up to 24 months]
To evaluate the duration of response according to the Investigator and Blinded Independent Central Review.
Disease Control Rate (DCR) [18 weeks from enrollment]
To evaluate patients disease control rate or complete response, partial response or stable disease at 18 weeks, as assessed by the Investigator.
Progression-Free Survival (PFS) [Enrollment through 24 months]
To evaluate progression-free survival, as assessed by the Investigator
Overall Survival (OS) [Enrollment through 24 months]
To evaluate overall survival.
Progression-Free Survival (PFS) [3 months, 6 months, and 12 months after Enrollment]
To evaluate progression-free survival at 3, 6 and 12 months
Overall Survival (OS) [3 months, 6 months, and 12 months after Enrollment]
To evaluate overall survival at 3, 6, and 12, months.
Cancer Antigen (CA)19-9 [8 and 16 weeks from Baseline]
To assess cancer antigen 19-9 (CA19-9) response at 8 and 16 weeks, in patients who have elevated CA19-9 at baseline.
Tumor Response per EORTC criteria [6 weeks post initiation of treatment]
To assess tumor response based on changes in FDG-PET scan at 6 weeks per the European Organization for Research and Treatment of Cancer (EORTC) criteria, according to the Blinded Independent Central Review (BICR)
Time to Progression (TTP) [From date of first treatment of relicorilant plus nab-paclitaxel until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months]
To evaluate the time to progression by comparing duration of disease control on prior nab-paclitaxel therapy (if applicable) and on the most recent therapy (study treatment of relacorilant and Nab-paclitaxel).

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria - Patients must have the following:

Histologically confirmed PDAC with metastatic disease. Received at least 2 prior lines of therapy for PDAC in any setting, including at least 1 prior gemcitabine-based therapy and at least 1 prior fluoropyrimidine-based therapy.

Received no more than 4 prior lines of cytotoxic or myelosuppressive therapy for PDAC.

A measurable lesion at baseline (within 21 days prior to the first dose of relacorilant) per RECIST v1.1, as assessed by the Investigator.

Willingness to provide blood samples and tumor tissue (primary or metastatic) for research purposes.

Karnofsky performance status (KPS) score of ≥70. Adequate gastrointestinal absorption. If the patient has undergone gastric bypass surgery and/or surgery of gastrointestinal or hepatobiliary tract, the patient must demonstrate adequate absorption as evidenced by albumin ≥3.0 g/dL, controlled pancreatic insufficiency (if present), and lack of evidence of malabsorption.

Adequate organ and marrow function (determined through blood and urine tests)

Exclusion Criteria - Patients must not have the following:

Pancreatic neuroendocrine tumors, lymphoma of the pancreas, acinar pancreatic cancer, or ampullary cancer.

Known untreated parenchymal brain metastasis or have uncontrolled central nervous system metastases. Patients must not require steroids and must be neurologically stable without corticosteroids for a minimum of 3 weeks prior to Cycle 1 Day 1.

Clinically relevant toxicity from prior systemic cytotoxic therapies or radiotherapy that in the opinion of the Investigator has not resolved to Grade 1 or less prior to enrollment, including peripheral neuropathy that is ongoing and greater than Grade 1 in severity, according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v5.0.

History of hypersensitivity or severe reaction to either relacorilant or nab-paclitaxel, or to similar classes of either drug.

Taken the following medications prior to enrollment:

An investigational product, cytotoxic chemotherapy or targeted agent within 14 days.
Radiotherapy within 21 days.
Palliative radiotherapy within 1 week of Cycle 1 Day 1, or if toxicities from radiotherapy are Grade 2 severity or higher or have not recovered to baseline.
Systemic or prescription strength topical corticosteroids for the purposes of treating a chronic nononcologic indication within 21 days.

Requirement for treatment with chronic or frequently used oral or inhaled corticosteroids for medical conditions or illnesses (e.g., rheumatoid arthritis, asthma, or immunosuppression after organ transplantation).

Taking a concomitant medication that is a strong CYP3A or CYP2C8 inhibitor or inducer, or a substrate of CYP3A (cytochrome P450 3A) or CYP2C8 (cytochrome P45 2C8) and has a narrow therapeutic window.

Concurrent treatment with mifepristone or other Glucocorticoid Receptor (GR) antagonists.

Any clinically significant uncontrolled condition(s) or any medical condition which in the opinion of the Investigator places the patient at an unacceptably high risk for toxicities or impair study participation or cooperation.

Any major surgery within 21 days prior to enrollment.

Endoscopic retrograde cholangiopancreatography with persistence of any of the following:

Bilirubin ≥1.5 × ULN (Upper Limit of Normal)
Amylase >2 × ULN and abdominal pain or amylase >3 × ULN (with or without symptoms)
Fever or signs of infection
Decreasing hemoglobin or signs of blood loss A history of human immunodeficiency virus (HIV) or current chronic/active infection with hepatitis C virus (HCV) or hepatitis B virus (HBV). (Patients with chronic or active hepatitis B as diagnosed by serologic tests are excluded from the study. In equivocal cases, hepatitis B or C polymerase chain reaction results may be performed and must be negative for enrollment.) A rapid decline in KPS score or serum albumin (≥20%), or have progressive pain symptoms indicative of rapid clinical deterioration, in the opinion of the Investigator, prior to enrollment. These patients will become ineligible if rapid decline is observed during the Screening Period.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Site #038	Scottsdale	Arizona	United States	85258
2	Site #171	Duarte	California	United States	91010
3	Site #076	Los Angeles	California	United States	90095
4	Site #032	Aurora	Colorado	United States	80045
5	Site #009	Atlanta	Georgia	United States	30322
6	Site #184	Goshen	Indiana	United States	46526
7	Site #065	Baltimore	Maryland	United States	21231
8	Site #058	Detroit	Michigan	United States	48201
9	Site #185	Omaha	Nebraska	United States	68114
10	Site #182	Buffalo	New York	United States	14263
11	Site #044	New York	New York	United States	10016
12	Site #222	New York	New York	United States	10016
13	Site #077	Columbus	Ohio	United States	43210
14	Site #186	Toledo	Ohio	United States	43614
15	Site #172	Pittsburgh	Pennsylvania	United States	15232
16	Site #175	Knoxville	Tennessee	United States	37920
17	Site #176	Nashville	Tennessee	United States	37232
18	Site #173	Seattle	Washington	United States	98195