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Completed Phase 2 Interventional Results available

Study Comparing Daratumumab, Lenalidomide, Bortezomib, and Dexamethasone (D-RVd) Versus Lenalidomide, Bortezomib, and Dexamethasone (RVd) in Subjects With Newly Diagnosed Multiple Myeloma

ClinicalTrials.gov ID: NCT02874742

Public ClinicalTrials.gov record NCT02874742. 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 Nov 7, 2026, 3:31 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase 2, Randomized, Open-Label Study Comparing Daratumumab, Lenalidomide, Bortezomib, and Dexamethasone (D-RVd) Versus Lenalidomide, Bortezomib, and Dexamethasone (RVd) in Subjects With Newly Diagnosed Multiple Myeloma Eligible for High-Dose Chemotherapy and Autologous Stem Cell Transplantation

Brief summary

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

The purpose of this study is to determine if the addition of daratumumab to lenalidomide-bortezomib-dexamethasone (RVd) will increase the proportion of participants achieving stringent complete response (sCR), as defined by the International Myeloma Working Group (IMWG) criteria, by the time of completion of post autologous stem cell transplantation (ASCT) consolidation treatment, compared with RVd alone.

Study identification

NCT ID
NCT02874742
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
224 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Aug 29, 2016 (Actual)
Primary completion
Jan 25, 2019 (Actual)
Completion
Apr 8, 2022 (Actual)
Last update posted
Feb 4, 2025

2016 – 2022

United States locations

U.S. sites
36
U.S. states
24
U.S. cities
36
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Duarte California — —
Not listed La Jolla California — —
Not listed Los Angeles California — —
Not listed San Francisco California — —
Not listed Aurora Colorado — —
Not listed Washington D.C. District of Columbia — —
Not listed Orlando Florida — —
Not listed Tampa Florida — —
Not listed Atlanta Georgia — —
Not listed Chicago Illinois — —
Not listed Westwood Kansas — —
Not listed New Orleans Louisiana — —
Not listed Baltimore Maryland — —
Not listed Boston Massachusetts — —
Not listed Worcester Massachusetts — —
Not listed Detroit Michigan — —
Not listed St Louis Missouri — —
Not listed Omaha Nebraska — —
Not listed Buffalo New York — —
Not listed New York New York — —
Not listed Chapel Hill North Carolina — —
Not listed Charlotte North Carolina — —
Not listed Durham North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Columbus Ohio — —
Not listed Portland Oregon — —
Not listed Abington Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed Salt Lake City Utah — —
Not listed Seattle Washington — —
Not listed Spokane Washington — —
Not listed Milwaukee Wisconsin — —

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 NCT02874742, 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 Feb 4, 2025 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02874742 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →