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Phase 2 Completed N=101 Treatment

A Study to Evaluate Dara-CyBorD in Previously Untreated and Relapsed Subjects With Multiple Myeloma

Source: ClinicalTrials.gov NCT02951819 ↗
Enrolled (actual)
101
Serious AEs
33.0%
Results posted
Apr 2019
Primary outcomePrimary: Percentage of Participants Who Achieved Complete Response (CR) or Very Good Partial Response (VGPR) — 44.2; 57.1 Percentage of Participants

Summary

The purpose of this study is to evaluate complete response plus (+) very good partial response (CR+VGPR) rate following 4 cycles of induction therapy of daratumumab in combination with cyclophosphamide, bortezomib, and dexamethasone (Dara-CyBorD), in previously untreated subjects, and in relapsed subjects with multiple myeloma, as defined by the International Myeloma Working Group (IMWG) criteria.

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants Who Achieved Complete Response (CR) or Very Good Partial Response (VGPR)
44.2; 57.1
SECONDARY
Overall Response Rate (ORR)
79.1; 71.4; 87.2; 78.6; 89.5; 85.7
SECONDARY
Time to Very Good Partial Response (VGPR) or Better
3.8; 1.8
SECONDARY
Time to Partial Response (PR) or Better
1.0; 1.0
SECONDARY
Duration of Response (DOR)
NA; 20.7
SECONDARY
Progression Free Survival (PFS)
NA; 21.7
SECONDARY
Time to Disease Progression (TTP)
NA; 13.31
SECONDARY
Overall Survival (OS)
NA; NA
SECONDARY
Percentage of Participants With Treatment Emergent-Adverse Event
100.0; 100.0

Eligibility Criteria

Inclusion Criteria

  • Subjects with documented multiple myeloma (MM) as defined by the International Myeloma Working Group (IMWG) 2015 criteria: Clonal bone marrow plasma cells greater than or equal to (>=) 10 percent (%) or biopsy-proven bony or extramedullary plasmacytoma and any one or more of the following CRAB (calcium level, renal dysfunction, anemia, and destructive bone lesions) features and myeloma defining events as in the protocol
  • Subjects with previously untreated myeloma or relapsed myeloma with one prior line of therapy including an induction regimen which may be followed by autologous stem cell transplantation and single agent maintenance therapy. For previously untreated subjects an emergency course of steroids (defined as no greater than 40 milligram (mg) of dexamethasone, or equivalent per day for a maximum of 4 days) is permitted. In addition, radiation therapy is permitted prior to study entry, during screening, and during Cycles 1-2 of study treatment as needed for lytic bone disease
  • Have an Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1, or 2
  • A woman of childbearing potential must have 2 negative serum (beta (β) human chorionic gonadotropin) or urine pregnancy tests during screening, the first one within 28 days prior to the first dose of study drug and the second within 24 hours prior to the first dose of study drug
  • A man who is sexually active with a woman of childbearing potential and has not had a vasectomy must agree to use a barrier method of birth control example, either condom with spermicidal foam/gel/film/cream/suppository or partner with occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository, and all men must also not donate sperm during the study and for 3 months after receiving the last dose of study drug

Exclusion Criteria

  • Refractory to any proteasome inhibitor (PI) or the combination of PI and immunomodulatory drug (IMiD) agents (such as lenalidomide), defined as failure to respond or progression within 60 days of the end of PI therapy
  • Exhibiting clinical signs of or has a known history of meningeal or central nervous system involvement by multiple myeloma
  • Has known chronic obstructive pulmonary disease with a forced expiratory volume in 1 second (FEV1) less than (<) 50 percent (%) of predicted normal
  • Has known moderate or severe persistent asthma within the past 2 years, or currently has uncontrolled asthma of any classification
  • Is known to be seropositive for human immunodeficiency virus, known to have hepatitis B surface antigen positivity, or known to have a history of hepatitis C
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02951819). 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.

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