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Terminated Phase 3 Interventional

RRx-001 Sequentially With a Platinum Doublet or a Platinum Doublet in Third-Line or Beyond in Patients With Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT03699956

Public ClinicalTrials.gov record NCT03699956. 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 4, 2026, 6:49 AM 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, Controlled, Open-label, Randomized Study of RRx-001 Administered Sequentially With a Platinum Doublet or a Platinum Doublet in Third-Line or Beyond Small Cell Lung Cancer

Brief summary

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

This Phase 3 study aims to find out whether RRx-001 + platinum chemotherapy is more effective than platinum chemotherapy alone in 3rd line or beyond small cell cancer.

Study identification

NCT ID
NCT03699956
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
EpicentRx, Inc.
Industry
Enrollment
18 participants

Conditions and interventions

Interventions

Combination Product · Drug

Eligibility (public fields only)

Age range
18 Years to 79 Years
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
Dec 23, 2018
Primary completion
Aug 10, 2022
Completion
Feb 29, 2024
Last update posted
Mar 25, 2024

2018 – 2024

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Centura Health Research Center Denver Colorado 80210
Mid Florida Hematology and Oncology Center Orange City Florida 32763
AdventHealth Hematology and Oncology Orlando Florida 32804
H. Lee Moffitt Cancer Center & Research Institute, Inc. Tampa Florida 33612
Rush University Medical Center Chicago Illinois 60612
Cotton O'Neil Clinical Research Center.Hematology & Oncology Topeka Kansas 66606
The University of Kansas Cancer Center Westwood Kansas 66205
Norton Cancer Institute, Norton Healthcare Pavilion Louisville Kentucky 40202
University of Maryland Marlene and Stewart Greenbaum Comprehensive Cancer Center Baltimore Maryland 21201
University of Mississippi Medical Center Jackson Mississippi 39213
Washington University School of Medicine - Siteman Cancer Center St Louis Missouri 63110
Oncology Hematology West PC dba Nebraska Cancer Specialists Omaha Nebraska 68124
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756
Stephenson Cancer Center Oklahoma City Oklahoma 73104
Tennessee Cancer Specialists Knoxville Tennessee 37909
Millennium Oncology Houston Texas 77090
HOPE Cancer Center of East Texas Tyler Texas 75701
Utah Cancer Specialist Salt Lake City Utah 84106

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 NCT03699956, 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, 2024 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03699956 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →