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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 May 6, 2026, 8:28 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

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

Study identification

NCT ID
NCT02874742
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
224 participants

Conditions and interventions

Interventions

  • Bortezomib Drug
  • Daratumumab Drug
  • Dexamethasone Drug
  • Lenalidomide Drug

Drug

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 28, 2016
Primary completion
Jan 24, 2019
Completion
Apr 7, 2022
Last update posted
Feb 3, 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 3, 2025 · Synced May 6, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02874742 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →