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Completed Phase 2 Interventional Results available

A Study to Evaluate Dara-CyBorD in Previously Untreated and Relapsed Subjects With Multiple Myeloma

ClinicalTrials.gov ID: NCT02951819

Public ClinicalTrials.gov record NCT02951819. 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 Sep 12, 2026, 9:29 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

Daratumumab Plus Cyclophosphamide, Bortezomib and Dexamethasone (Dara-CyBorD) in Previously Untreated and Relapsed Subjects With Multiple Myeloma

Brief summary

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

The purpose of this study is to evaluate complete response plus (+) very good partial response (CR+VGPR) rate following 4 cycles of induction therapy of daratumumab in combination with cyclophosphamide, bortezomib, and dexamethasone (Dara-CyBorD), in previously untreated subjects, and in relapsed subjects with multiple myeloma, as defined by the International Myeloma Working Group (IMWG) criteria.

Study identification

NCT ID
NCT02951819
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Janssen Scientific Affairs, LLC
Industry
Enrollment
101 participants

Conditions and interventions

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
Nov 8, 2016
Primary completion
Mar 7, 2018
Completion
Aug 16, 2020
Last update posted
Oct 7, 2021

2016 – 2020

United States locations

U.S. sites
26
U.S. states
18
U.S. cities
26
Facility City State ZIP Site status
Not listed Mobile Alabama
Not listed Phoenix Arizona
Not listed Sedona Arizona
Not listed Tucson Arizona
Not listed Fayetteville Arkansas
Not listed Greenbrae California
Not listed Denver Colorado
Not listed Niles Illinois
Not listed Indianapolis Indiana
Not listed Louisville Kentucky
Not listed Bethesda Maryland
Not listed Columbia Maryland
Not listed Grand Rapids Michigan
Not listed Omaha Nebraska
Not listed Camden New Jersey
Not listed Albany New York
Not listed East Setauket New York
Not listed Fresh Meadows New York
Not listed Cincinnati Ohio
Not listed Eugene Oregon
Not listed Greenville South Carolina
Not listed Austin Texas
Not listed Dallas Texas
Not listed San Antonio Texas
Not listed Tyler Texas
Not listed Seattle Washington

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02951819, 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 Oct 7, 2021 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02951819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →