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NCT03610711 · ClinicalTrials.gov registry record · Phase 1

REACTION (Radiation Enhanced Assessment of Combination Therapies in Immuno-ONcology) - Nivolumab or Nivolumab in Combination With Other Immuno-oncology (IO) Agents After Targeted Systemic Radiation in Patients With Advanced Esophagogastric Cancer

A Phase 1 study of GastroEsophageal Cancer and Immune Checkpoint Inhibition, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Active
Registry status
Phase 1
Development phase
21
Enrollment target
3
Study locations

NCT03610711 is a Phase 1 study of GastroEsophageal Cancer and Immune Checkpoint Inhibition that is active but no longer recruiting, run by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. The registered enrollment target is 21 participants, below the 496-participant average among 23 other GastroEsophageal Cancer trials with a reported enrollment target (96% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT03610711, a Phase 1 study of GastroEsophageal Cancer and Immune Checkpoint Inhibition, is active but no longer recruiting, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

ACTIVE NOT RECRUITING
Registry status
Phase 1
Development phase
21 participants
Enrollment target
3
Study locations

Study Summary

This is a Phase 1B study assessing the safety of immune checkpoint inhibition after SBRT in patients with recurrent or metastatic gastroesophageal cancer (limited metastatic disease).

Interventions

  • DRUG Nivolumab
  • DRUG Relatlimab

Study Locations (3)

Maryland

  • Johns Hopkins University - Baltimore

Pennsylvania

  • Alleghany Health Network - Pittsburgh

Texas

  • Baylor University - Dallas

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2019-03-06
Est. Completion 2026-12
Phase Phase 1

What the Registry Record Tells You About NCT03610711

The ClinicalTrials.gov registry entry for NCT03610711 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 496-participant average among 23 other GastroEsophageal Cancer trials with a reported enrollment target (96% lower). The listed sponsor is Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with GastroEsophageal Cancer appearing as the primary indexed condition, and to 2 interventions - of which Nivolumab is the first listed.

NCT03610711 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Maryland, Pennsylvania, Texas.

Frequently Asked Questions

What is clinical trial NCT03610711 about?

NCT03610711 is a clinical study titled "REACTION (Radiation Enhanced Assessment of Combination Therapies in Immuno-ONcology) - Nivolumab or Nivolumab in Combination With Other Immuno-oncology (IO) Agents After Targeted Systemic Radiation in Patients With Advanced Esophagogastric Cancer". This is a Phase 1B study assessing the safety of immune checkpoint inhibition after SBRT in patients with recurrent or metastatic gastroesophageal cancer (limited metastatic disease).

What is the current status of trial NCT03610711?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2019-03-06. Estimated completion is 2026-12.

What conditions does trial NCT03610711 study?

This clinical trial studies the following conditions: GastroEsophageal Cancer, Immune Checkpoint Inhibition.

What interventions are being tested in trial NCT03610711?

The interventions under investigation include: Nivolumab (DRUG), Relatlimab (DRUG).

Who is sponsoring clinical trial NCT03610711?

This trial is sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, which has 523 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03610711 being conducted?

This trial has 3 study locations across Maryland, Pennsylvania, Texas. 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

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