Phase 2
Completed N=45
Daratumumab in Combination With Lenalidomide and Dexamethasone in Relapsed and Relapsed-refractory Multiple Myeloma
Source: ClinicalTrials.gov NCT01615029 ↗Enrolled (actual)
45
Serious AEs
68.9%
Results posted
Apr 2017
Primary outcomePrimary: Phase 1: Percentage of Participants With Overall Response Rate (ORR) — 100.0; 100.0; 75.0; 66.7 Percentage of participants
Summary
The purpose of this study is to establish the safety profile of daratumumab when given in combination with Lenalidomide and dexamethasone in participants with relapsed or relapsed and refractory Multiple Myeloma (MM).
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Phase 1: Percentage of Participants With Overall Response Rate (ORR) |
100.0; 100.0; 75.0; 66.7; 85.4 | — |
| PRIMARY Phase 2: Percentage of Participants With Overall Response Rate (ORR) |
81.3 | — |
| SECONDARY Phase 2: Duration of Response |
NA | — |
| SECONDARY Phase 1: Time to Response |
0.99; 1.02; 1.02; 2.25; 1.9; 13.17 | — |
| SECONDARY Phase 2: Time to Response |
0.99; 6.95 | — |
| SECONDARY Phase 2: Time to Progression (TTP) |
NA | — |
| SECONDARY Phase 2: Progression-Free Survival (PFS) |
NA | — |
| SECONDARY Phase 2: Overall Survival (OS) |
NA | — |
Eligibility Criteria
Inclusion Criteria
- (Part 1) Have relapsed multiple myeloma after receiving a minimum of 2 and a maximum of 4 prior lines of therapy and be eligible for treatment with lenalidomide and dexamethasone (Len/Dex)
- (Part 2) Have received at least 1 prior line of therapy for multiple myeloma
- Be older than or be 18 years of age
- Eastern Cooperative Oncology Group (ECOG) performance status (0-2)
- Provide signed informed consent after receipt of oral and written information about the study and before any study-related activity is performed
Exclusion Criteria
- Have previously received an allogenic stem cell transplant
- Have received autologous stem cell transplant within 12 weeks before the first infusion
- Have received antimyeloma treatment, radiotherapy, or any experimental drug or therapy within 2 weeks before the first infusion
- Have discontinued lenalidomide due to any treatment-related adverse event or be refractory to any dose of lenalidomide. Refractory to lenalidomide is defined as either, participants whose disease progresses within 60 days of lenalidomide, or participants whose disease is nonresponsive while on any dose of lenalidomide. Nonresponsive disease is defined as either failure to achieve at least an minimal response (MR) or development of progressive disease (PD) while on lenalidomide
Data sourced from ClinicalTrials.gov (NCT01615029). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.