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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 Oct 28, 2026, 5:41 AM 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 9, 2016 (Actual)
Primary completion
Mar 8, 2018 (Actual)
Completion
Aug 17, 2020 (Actual)
Last update posted
Oct 8, 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 8, 2021 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02951819 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →