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NCT02899052Active, not recruitingPhase 2

Study of Venetoclax in Combination With Carfilzomib and Dexamethasone in Participants With Relapsed or Refractory Multiple Myeloma (MM)

A Phase 2, Open-Label, Multi-Center Study of Venetoclax in Combination With Carfilzomib and Dexamethasone in Subjects With Relapsed or Refractory Multiple Myeloma

Source: ClinicalTrials.gov · Last updated 5 Aug 2025

Brief summary (registry, in English)

A Phase 2, open-label, dose escalation study to evaluate the safety and efficacy of venetoclax in combination with carfilzomib-dexamethasone (Kd) in participants with relapsed or refractory MM and have received 1 to 3 prior lines of therapy. Part 4 of this study is currently enrolling.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
120 (estimated)
First submitted
1 Sept 2016
Start date
19 Jan 2017
Primary completion date
30 Jun 2027
Lead sponsor
AbbVie
NCT number
NCT02899052
EU CT number
2023-505659-27-00
EudraCT number
2019-004340-30

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 120
  • From 19 Jan 2017 to the primary completion date, 30 Jun 2027
  • 32 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has a pre-existing condition that is contraindicated including.
    • Non-secretory or oligo-secretory MM
    • Active plasma cell leukemia.
    • Waldenström's macroglobulinemia.
    • Primary amyloidosis.
    • POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes).
    • Active hepatitis B or C infection based on screening blood testing.
    • Known active Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.
    • Significant cardiovascular disease.
    • Major surgery within 4 weeks prior to first dose.
    • Acute infections requiring antibiotic, antifungal or antiviral therapy within14 days prior to first dose.
    • Peripheral neuropathy ≥ Grade 3 or ≥ Grade 2 with pain within 2 weeks prior to first dose.
    • Uncontrolled diabetes or uncontrolled hypertension within 14 days prior to first dose.
    • Any other medical condition that, in the opinion of the Investigator, would adversely affect the participant's participation in the study.
  • History of other active malignancies, including myelodysplastic syndrome (MDS), within the past 3 years prior to study entry Other protocol defined inclusion/exclusion criteria could apply

Who the study is looking for

  • Eastern Collaborative Oncology Group (ECOG) performance score of less than or equal to 2.
  • Documented relapsed or progressive Multiple Myeloma (MM) on or after any regimen or is refractory to the most recent line of therapy.
  • Positive for translocation t(11;14) as determined by an analytically validated Fluorescent In Situ Hybridization (FISH) assay per central laboratory testing.
  • Received prior treatment with at least 1 prior line of therapy for MM.
  • Measurable disease on Screening per International Myeloma Working Group (IMWG) criteria.
  • Meets absolute neutrophil count, platelet count, hemoglobin, liver and kidney function laboratory values within 2 weeks prior to first dose of study drug.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (32)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Flinders Medical Centre /ID# 221345
Coordinator of this site? Confirm its status
Bedford ParkAustraliaUnknown status
Border Medical Oncology Research Unit Albury Wodonga Regiona /ID# 222200
Coordinator of this site? Confirm its status
East AlburyAustraliaUnknown status
Royal Hobart Hospital /ID# 217546
Coordinator of this site? Confirm its status
HobartAustraliaUnknown status
Calvary Mater Newcastle /ID# 218739
Coordinator of this site? Confirm its status
WaratahAustraliaUnknown status
Hospital Germans Trias i Pujol
Coordinator of this site? Confirm its status
BadalonaSpainActive, not recruiting
Hospital Clinic de Barcelona
Coordinator of this site? Confirm its status
BarcelonaSpainActive, not recruiting
Hospital Universitario Ramón y Cajal
Coordinator of this site? Confirm its status
MadridSpainActive, not recruiting
Hospital General Universitario Gregorio Marañón
Coordinator of this site? Confirm its status
MadridSpainActive, not recruiting
Del-Pesti Centrumkorhaz Orszagos Hematologiai Es Infektologiai Intezet
Coordinator of this site? Confirm its status
Budapest IXHungaryCompleted
Semmelweis University
Coordinator of this site? Confirm its status
Budapest VIIIHungaryCompleted
University of Debrecen
Coordinator of this site? Confirm its status
DebrecenHungaryCompleted
University of Szeged
Coordinator of this site? Confirm its status
SzegedHungaryCompleted
VA Caribbean Healthcare System /ID# 157854
Coordinator of this site? Confirm its status
San JuanPuerto RicoUnknown status
Auxilio Mutuo Cancer Center /ID# 157853
Coordinator of this site? Confirm its status
San JuanPuerto RicoUnknown status
Winship Cancer Institute of Emory University /ID# 161710
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
Duplicate_University of Maryland School of Medicine /ID# 159721
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
University of Alabama at Birmingham - Main /ID# 151405
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BirminghamUnited StatesUnknown status
The University of Chicago Medical Center /ID# 151395
Coordinator of this site? Confirm its status
ChicagoUnited StatesUnknown status
University of Texas Southwestern Medical Center /ID# 218336
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DallasUnited StatesUnknown status
Duke Cancer Center /ID# 162062
Coordinator of this site? Confirm its status
DurhamUnited StatesUnknown status
Memorial Healthcare System /ID# 224862
Coordinator of this site? Confirm its status
HollywoodUnited StatesUnknown status
Indiana Blood & Marrow Transpl /ID# 218862
Coordinator of this site? Confirm its status
IndianapolisUnited StatesUnknown status
Central Maine Medical Center /ID# 218856
Coordinator of this site? Confirm its status
LewistonUnited StatesUnknown status
Duplicate_University of Kentucky Chandler Medical Center /ID# 151407
Coordinator of this site? Confirm its status
LexingtonUnited StatesUnknown status
University of Arkansas for Medical Sciences /ID# 151399
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Little RockUnited StatesUnknown status
University of Pennsylvania /ID# 151768
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PhiladelphiaUnited StatesUnknown status
University of Utah /ID# 151397
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesUnknown status
Duplicate_VA Puget Sound Healthcare Syst /ID# 155369
Coordinator of this site? Confirm its status
SeattleUnited StatesUnknown status
Oncology Hematology Associates (OHA) - Springfield /ID# 218855
Coordinator of this site? Confirm its status
SpringfieldUnited StatesUnknown status
Washington University-School of Medicine /ID# 222651
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Baylor Scott & White Medical Center- Temple /ID# 218252
Coordinator of this site? Confirm its status
TempleUnited StatesUnknown status
Aurora Health Care, Aurora Cancer Center /ID# 209612
Coordinator of this site? Confirm its status
WauwatosaUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.