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Completed Phase 2 Interventional Results available

An Investigational Immuno-therapy Trial of Pomalidomide and Low-dose Dexamethasone With or Without Elotuzumab to Treat Refractory and Relapsed and Refractory Multiple Myeloma (ELOQUENT-3)

ClinicalTrials.gov ID: NCT02654132

Public ClinicalTrials.gov record NCT02654132. 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 Oct 21, 2026, 12:43 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open Label, Randomized Phase 2 Trial of Pomalidomide/Dexamethasone With or Without Elotuzumab in Relapsed and Refractory Multiple Myeloma (ELOQUENT-3)

Brief summary

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

The purpose of this study is to determine if adding Elotuzumab to Pomalidomide and low-dose dexamethasone is a more effective treatment of relapsed and refractory multiple myeloma compared to pomalidomide and low-dose dexamethasone by itself.

Study identification

NCT ID
NCT02654132
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
117 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Mar 18, 2016 (Actual)
Primary completion
Jan 17, 2018 (Actual)
Completion
Oct 21, 2021 (Actual)
Last update posted
Nov 1, 2022

2016 – 2021

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
11
Facility City State ZIP Site status
Winship Cancer Institute Atlanta Georgia 30322 —
Rush University Medical Center Chicago Illinois 60612 —
Investigative Clinical Research Of Indiana, Llc Indianapolis Indiana 46260 —
Beth Israel Comprehensive Cancer Center Boston Massachusetts 02215 —
Dana Farber Cancer Institute. Boston Massachusetts 02215 —
Rochester General Hospital Rochester New York 14621 —
Carolinas Healthcare System Charlotte North Carolina 28204 —
Va Pittsburgh Healthcare System Pittsburgh Pennsylvania 15240 —
St Francis Hospital Greenville South Carolina 29607 —
Tennessee Cancer Specialists Knoxville Tennessee 37909 —
Northern Utah Associates Ogden Utah 84403 —
University Of Washington Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 43 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02654132, 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 Nov 1, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02654132 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →