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Corticosteroid

Elotuzumab + Pomalidamide + Low Dose Dexamethasone (EPd) for Multiple Myeloma

Phase 2
Waitlist Available
Research Sponsored by Bristol-Myers Squibb
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from first dose to study completion date (up to approximately 50 months)
Awards & highlights
All Individual Drugs Already Approved
Approved for 60 Other Conditions
No Placebo-Only Group

Summary

Study of elotuzumab in combination with pomalidomide and low dose dexamethasone (EPd Cohort) and elotuzumab in combination with nivolumab (EN Cohort) to assess the safety and efficacy of these combination therapies for treatment of relapsed or refractory MM patients.

Eligible Conditions
  • Multiple Myeloma

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from first dose to study completion date (up to approximately 50 months)
This trial's timeline: 3 weeks for screening, Varies for treatment, and from first dose to study completion date (up to approximately 50 months) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
Objective Response Rate (ORR)
Overall Survival (OS)
Progression Free Survival (PFS)

Awards & Highlights

All Individual Drugs Already Approved
Therapies where all constituent drugs have already been approved are likely to have better-understood side effect profiles.
Approved for 60 Other Conditions
This treatment demonstrated efficacy for 60 other conditions.
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Group I: Elotuzumab + Pomalidamide + Low Dose Dexamethasone (EPd)Experimental Treatment4 Interventions
patients will receive treatment with elotuzumab in combination with pomalidomide and low-dose dexamethasone. Patients are eligible to receive Nivolumab at progression.
Group II: Elotuzumab + Nivolumab (EN)Experimental Treatment2 Interventions
Patients will receive treatment with a combination of elotuzumab and nivolumab
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Elotuzumab
FDA approved
Pomalidomide
FDA approved
Dexamethasone
FDA approved
Nivolumab
FDA approved

Find a Location

Who is running the clinical trial?

Bristol-Myers SquibbLead Sponsor
2,685 Previous Clinical Trials
4,129,509 Total Patients Enrolled
90 Trials studying Multiple Myeloma
22,359 Patients Enrolled for Multiple Myeloma
Bristol Myers SquibbStudy DirectorBristol-Myers Squibb
31 Previous Clinical Trials
32,460 Total Patients Enrolled
~8 spots leftby Nov 2025