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Alkylating Agent
Nivolumab for Multiple Myeloma
Phase 2
Waitlist Available
Research Sponsored by Andrew Yee, MD
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 up to 2 years
Awards & highlights
Study Summary
This trial is testing a new combination treatment for multiple myeloma that has relapsed or become resistant to other treatments.
Eligible Conditions
- Multiple Myeloma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Objective Response Rate (ORR)
Secondary outcome measures
Progression Free Survival
Trial Design
1Treatment groups
Experimental Treatment
Group I: Nivolumab and IxazomibExperimental Treatment4 Interventions
- Participants will receive Nivolumab, Ixazomib, Cyclophosphamide, and Dexamethasone on a 28-day cycle.
Oral:
Ixazomib given weekly on days 1, 8, 15
Dexamethasone given weekly during cycle
Infused:
Nivolumab given once per cycle
Cyclophosphamide given on days 1, 8, 15 during cycle
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Nivolumab
FDA approved
Ixazomib
FDA approved
Dexamethasone
FDA approved
Cyclophosphamide
FDA approved
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Who is running the clinical trial?
Andrew Yee, MDLead Sponsor
1 Previous Clinical Trials
43 Total Patients Enrolled
1 Trials studying Multiple Myeloma
43 Patients Enrolled for Multiple Myeloma
Bristol-Myers SquibbIndustry Sponsor
2,650 Previous Clinical Trials
4,130,830 Total Patients Enrolled
88 Trials studying Multiple Myeloma
30,531 Patients Enrolled for Multiple Myeloma
Takeda Pharmaceuticals North America, Inc.Industry Sponsor
57 Previous Clinical Trials
8,961 Total Patients Enrolled
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