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NCT04021108 · ClinicalTrials.gov registry record · Phase 2

Phase II Study of Short Course FOLFOX Chemotherapy With Either Nivolumab or Nivolumab + Radiation in the First Line Treatment of Metastatic or Unresectable Gastroesophageal Cancers (BMS Protocol CA209-76L)

A Phase 2 study of Gastroesophageal Adenocarcinoma, sponsored by Weill Medical College of Cornell University.

Active
Registry status
Phase 2
Development phase
80
Enrollment target
5
Study locations

NCT04021108 is a Phase 2 study of Gastroesophageal Adenocarcinoma that is active but no longer recruiting, run by Weill Medical College of Cornell University. The registered enrollment target is 80 participants, below the 141-participant average among 8 other Gastroesophageal Adenocarcinoma trials with a reported enrollment target (43% lower). The trial reports 5 study locations across 4 states.

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The verdict

NCT04021108, a Phase 2 study of Gastroesophageal Adenocarcinoma, is active but no longer recruiting, sponsored by Weill Medical College of Cornell University.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
80 participants
Enrollment target
5
Study locations

Study Summary

This is a randomized phase II study examining nivolumab alone versus radiation therapy with nivolumab in subjects who did not have disease progression to initial therapy with the combination of FOLFOX and Nivolumab.

Interventions

  • DRUG Nivolumab 240 MG

Study Locations (5)

New York

  • Roswell Park Cancer Center - Buffalo
  • Weill Cornell Medicine - New York

Florida

  • Moffitt Cancer Center - Tampa

Missouri

  • Washington University School of Medicine - St Louis

Nebraska

  • University of Nebraska - Omaha

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2019-07-22
Est. Completion 2026-06
Phase Phase 2

What the Registry Record Tells You About NCT04021108

The ClinicalTrials.gov registry entry for NCT04021108 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 141-participant average among 8 other Gastroesophageal Adenocarcinoma trials with a reported enrollment target (43% lower). The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Gastroesophageal Adenocarcinoma appearing as the primary indexed condition, and to 1 intervention - of which Nivolumab 240 MG is the first listed.

NCT04021108 reports 5 study locations spanning 4 distinct geographic areas - top geographies include New York, Florida, Missouri.

Frequently Asked Questions

What is clinical trial NCT04021108 about?

NCT04021108 is a clinical study titled "Phase II Study of Short Course FOLFOX Chemotherapy With Either Nivolumab or Nivolumab + Radiation in the First Line Treatment of Metastatic or Unresectable Gastroesophageal Cancers (BMS Protocol CA209-76L)". This is a randomized phase II study examining nivolumab alone versus radiation therapy with nivolumab in subjects who did not have disease progression to initial therapy with the combination of FOLFOX and Nivolumab.

What is the current status of trial NCT04021108?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 80 participants. The study started on 2019-07-22. Estimated completion is 2026-06.

What conditions does trial NCT04021108 study?

This clinical trial studies the following conditions: Gastroesophageal Adenocarcinoma.

What interventions are being tested in trial NCT04021108?

The interventions under investigation include: Nivolumab 240 MG (DRUG).

Who is sponsoring clinical trial NCT04021108?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04021108 being conducted?

This trial has 5 study locations across Florida, Missouri, Nebraska, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.