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NCT01615029CompletedPhase 1/2

Daratumumab in Combination With Lenalidomide and Dexamethasone in Relapsed and Relapsed-refractory Multiple Myeloma

An Open Label, International, Multicenter, Dose Escalating Phase I/II Trial Investigating the Safety of Daratumumab in Combination With Lenalidomide and Dexamethasone in Patients With Relapsed or Relapsed and Refractory Multiple Myeloma

Source: ClinicalTrials.gov · Last updated 16 Mar 2026

Brief summary (registry, in English)

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).

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
45 (actual)
First submitted
6 Jun 2012
Start date
26 Jun 2012
Primary completion date
2 Oct 2015
Lead sponsor
Janssen Research & Development, LLC
NCT number
NCT01615029
EudraCT number
2011-005709-62

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 45
  • From 26 Jun 2012 to the primary completion date, 2 Oct 2015
  • 8 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

  • 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

Other illness

  • 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

Who the study is looking for

  • (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

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

Full criteria on ClinicalTrials.gov

Sites (8)

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

SiteCityCountrySite status
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Coordinator of this site? Confirm its status
Copenhagen ØDenmarkUnknown status
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VejleDenmarkUnknown status
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Coordinator of this site? Confirm its status
LilleFranceUnknown status
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Coordinator of this site? Confirm its status
NantesFranceUnknown status
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Coordinator of this site? Confirm its status
Vandœuvre-lès-NancyFranceUnknown status
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Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status
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Coordinator of this site? Confirm its status
UtrechtNetherlandsUnknown status
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Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

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