CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 82 enrolled
Drug / intervention
Nivolumab +4 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02275533
NCT02275533Phase 2Active

Randomized Phase II Study to Assess the Role of Nivolumab as Single Agent to Eliminate Minimal Residual Disease and Maintain Remission in Acute Myelogenous Leukemia (AML) Patients After Chemotherapy (REMAIN TRIAL)

National Cancer Institute (NCI)·interventional·Posted Oct 27, 2014·Updated May 28, 2026

In Brief

A Phase 2 clinical trial evaluating Biospecimen Collection, Bone Marrow Biopsy, and 3 other interventions for Acute Myeloid Leukemia. Active but no longer recruiting, targeting 82 participants across 46 sites in 2 countries.

Detailed Summary

This phase II trial studies how well nivolumab works in eliminating any remaining cancer cells and preventing cancer from returning in patients with acute myeloid leukemia that had a decrease in or disappearance of signs and symptoms of cancer after receiving chemotherapy. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
Collaborators--

Timeline

Phase 2Active
2015201620172018201920202021202220232024202520262027
First PostedOct 27, 2014
Enrollment StartJul 2, 2015
Primary CompletionJul 28, 2025
Study CompletionOct 8, 2026
TodayJul 2, 2026
Enrollment to primary: 10.1 yearsPosted 11.7 years ago

Interventions

Biospecimen Collectionprocedure

Undergo collection of blood samples

Bone Marrow Biopsyprocedure

Undergo bone marrow biopsy

Clinical Observationother

Undergo standard of care clinical observation

Echocardiography Testprocedure

Undergo ECHO

Nivolumabbiological

Given IV