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
- Diseases
- Multiple myeloma
- 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
Sites (8)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| - Coordinator of this site? Confirm its status | Copenhagen Ø | Denmark | Unknown status |
| - Coordinator of this site? Confirm its status | Vejle | Denmark | Unknown status |
| - Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| - Coordinator of this site? Confirm its status | Nantes | France | Unknown status |
| - Coordinator of this site? Confirm its status | Vandœuvre-lès-Nancy | France | Unknown status |
| - Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| - Coordinator of this site? Confirm its status | Utrecht | Netherlands | Unknown status |
| - Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.