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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 Sep 2, 2026, 3:15 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
Oct 31, 2016
Primary completion
Jan 21, 2025
Completion
Jan 21, 2025
Last update posted
Mar 25, 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.

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Other public records listing Lung Cancer. Sorted by last update posted; newest first. Not a recommendation.

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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 25, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02922764 live on ClinicalTrials.gov.

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