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NCT03607890 · ClinicalTrials.gov registry record · Phase 2

Study of Nivolumab and Relatlimab in Advanced Mismatch Repair Deficient Cancers Resistant to Prior PD-(L)1 Inhibitor

A Phase 2 study of Refractory MSI - H Solid Tumors Prior of PD-(L) 1 Therapy and MSI-H Tumors, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Active
Registry status
Phase 2
Development phase
38
Enrollment target
2
Study locations

NCT03607890 is a Phase 2 study of Refractory MSI - H Solid Tumors Prior of PD-(L) 1 Therapy and MSI-H Tumors that is active but no longer recruiting, run by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. The registered enrollment target is 38 participants. The trial reports 2 study locations across 2 states.

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The verdict

NCT03607890, a Phase 2 study of Refractory MSI - H Solid Tumors Prior of PD-(L) 1 Therapy and MSI-H Tumors, is active but no longer recruiting, sponsored by Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

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

Study Summary

The purpose of this study is to evaluate the safety and clinical activity of nivolumab and relatlimab in patients with microsatellite instability high (MSI-H) solid tumors refractory to prior PD-(L)1 therapy.

Interventions

  • DRUG Nivolumab
  • DRUG Relatlimab

Study Locations (2)

California

  • Cedars Sinai Medical Center - Los Angeles

Maryland

  • Sidney Kimmel Comprehensive Cancer Center - Baltimore

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2018-11-16
Est. Completion 2026-10
Phase Phase 2

What the Registry Record Tells You About NCT03607890

The ClinicalTrials.gov registry entry for NCT03607890 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. 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 Refractory MSI - H Solid Tumors Prior of PD-(L) 1 Therapy appearing as the primary indexed condition, and to 2 interventions - of which Nivolumab is the first listed.

NCT03607890 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, Maryland.

Frequently Asked Questions

What is clinical trial NCT03607890 about?

NCT03607890 is a clinical study titled "Study of Nivolumab and Relatlimab in Advanced Mismatch Repair Deficient Cancers Resistant to Prior PD-(L)1 Inhibitor". The purpose of this study is to evaluate the safety and clinical activity of nivolumab and relatlimab in patients with microsatellite instability high (MSI-H) solid tumors refractory to prior PD-(L)1 therapy.

What is the current status of trial NCT03607890?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 38 participants. The study started on 2018-11-16. Estimated completion is 2026-10.

What conditions does trial NCT03607890 study?

This clinical trial studies the following conditions: Refractory MSI - H Solid Tumors Prior of PD-(L) 1 Therapy, MSI-H Tumors.

What interventions are being tested in trial NCT03607890?

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

Who is sponsoring clinical trial NCT03607890?

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 NCT03607890 being conducted?

This trial has 2 study locations across California, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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.