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Active, not recruiting Phase 2 Interventional

Study of Selinexor Plus DRd for Newly Diagnosed Multiple Myeloma

ClinicalTrials.gov ID: NCT04782687

Public ClinicalTrials.gov record NCT04782687. 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 23, 2026, 4:00 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

A Phase II Trial of Daratumumab, Lenalidomide and Dexamethasone (DRd) in Combination With Selinexor for Patients With Newly Diagnosed Multiple Myeloma

Brief summary

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

This is a single-arm, phase II, open-label trial to investigate the effects of selinexor (S) in combination with daratumumab, lenalidomide, and dexamethasone (DRd) for first-line treatment of multiple myeloma (MM). FDA has approved selinexor plus dexamethasone in multiple myeloma after four prior therapies, and DRd is also already approved by the FDA for multiple myeloma. This study will use all four (S-DRd) together to treat MM as an initial treatment.

Study identification

NCT ID
NCT04782687
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
US Oncology Research
Industry
Enrollment
73 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
Sep 10, 2021 (Actual)
Primary completion
May 31, 2026 (Estimated)
Completion
May 31, 2026 (Estimated)
Last update posted
Jan 16, 2025

2021 – 2026

United States locations

U.S. sites
10
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Arizona Oncology Associates, PC - HOPE Tucson Arizona 85711 —
Rocky Mountain Cancer Centers Denver Colorado 80218 —
Maryland Oncology Hematology, P.A. Columbia Maryland 21044 —
New York Oncology Hematology, P.C. Albany New York 12206 —
Willamette Valley Cancer Institute and Research Center Eugene Oregon 97401 —
Texas Oncology, P.A. Austin Texas 78705 —
Texas Oncology, P.A. Fort Worth Texas 76104 —
Texas Oncology, P.A. San Antonio Texas 78240 —
Texas Oncology, P.A. Tyler Texas 75702 —
Virginia Cancer Specialists, PC Gainesville Virginia 20155 —

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 NCT04782687, 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 Jan 16, 2025 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04782687 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →