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A Study of Combination Therapy With Venetoclax, Daratumumab and Dexamethasone (With and Without Bortezomib) in Participants With Relapsed or Refractory Multiple Myeloma

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NCT03314181 · readout ≤ 1,746 d

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →. With Janssen Research & Development, LLC.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
156actual
Sites
40
Countries
Australia, Canada, Denmark +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2018-04-02actualWhen the study began enrolling
Primary completionMay 2031estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionMay 2031estimatedThe whole study's end, after follow-up
First posted2017-10-19actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-08-14actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Multiple Myeloma

Interventions

  • Drug: Dexamethasone
  • Drug: Daratumumab
  • Drug: Venetoclax — also filed as ABT-199, Venclexta
  • Drug: Bortezomib

Primary outcomes

what the primary-completion date above is the date OF
Overall Response Rate (ORR)
measured Up to approximately 3.5 years after the last participant is enrolled
Very Good Partial Response or Better Response Rate (VGPR)
measured Up to approximately 3.5 years after the last participant is enrolled
Complete Response (CR) or Better Rate
measured Up to approximately 3.5 years after the last participant is enrolled
Time to Response (TTR)
measured Up to approximately 3.5 years after the last participant is enrolled
Duration of Response (DOR)
measured Up to approximately 3.5 years after the last participant is enrolled
Time to Progression (TTP)
measured Up to approximately 3.5 years after the last participant is enrolled
Progression-Free Survival (PFS)
measured Up to approximately 3.5 years after the last participant is enrolled
Overall Survival (OS)
measured Up to approximately 3.5 years after the last participant is enrolled

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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