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Completed Phase 1 Interventional

A Study of RGX-104 in Patients With Advanced Lung & Endometrial Cancer

ClinicalTrials.gov ID: NCT02922764

Public ClinicalTrials.gov record NCT02922764. 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 17, 2026, 5:39 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 1 Study of RGX-104, a Small Molecule LXR Agonist, as a Single Agent and as Combination Therapy in Patients With Advanced Solid Malignancies and Expansion in Select Malignancies

Brief summary

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

Study RGX-104-001 is a Phase 1, first-in-human, dose escalation and expansion study of RGX-104, an oral small molecule targeting the liver X receptor (LXR), as a single agent and in combination with nivolumab, ipilimumab, docetaxel, or pembrolizumab plus carboplatin/pemetrexed.

Study identification

NCT ID
NCT02922764
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Inspirna, Inc.
Industry
Enrollment
146 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
Nov 1, 2016 (Actual)
Primary completion
Jan 22, 2025 (Actual)
Completion
Jan 22, 2025 (Actual)
Last update posted
Mar 26, 2025

2016 – 2025

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
Arizona Oncology Tucson Arizona 85711 —
Cedars-Sinai Medical Center Los Angeles California 90048 —
University of Colorado Aurora Colorado 80045 —
Rocky Mountain Cancer Centers Denver Colorado 80218 —
Sarah Cannon Research Institute Denver Colorado 80218 —
Florida Cancer Specialist Lake Mary Florida 32799 —
Comprehensive Hematology Oncology St. Petersburg Florida 33709 —
James Graham Brown Cancer Center Louisville Kentucky 40202 —
Ochsner Clinic Foundation New Orleans Louisiana 70121 —
Maryland Oncology Columbia Maryland 21044 —
Regions Hospital Saint Paul Minnesota 55101 —
Dartmouth Hitchcock Medical Lebanon New Hampshire 03756 —
CINJ New Brunswick New Jersey 08901 —
Quantum Santa Fe Santa Fe New Mexico 87505 —
Columbia University Medical Center New York New York 10032 —
OU Health Stephenson Cancer Center Oklahoma City Oklahoma 73104 —
Oregon Health Sciences University Portland Oregon 97239 —
Thomas Jefferson University Hospital Philadelphia Pennsylvania 19107 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
The Sarah Cannon Research Institute Nashville Tennessee 37203 —
Virginia Cancer Specialists, PC Fairfax Virginia 22031 —

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 NCT02922764, 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 Mar 26, 2025 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02922764 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →