Clinical trial · Interventional
Carfilzomib, Daratumumab, Lenalidomide and Dexamethasone as First Line Treatment in Multiple Myeloma
NCT04288765CI-TRIAL-00052608withdrawnPhase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): incomplete recruitment
Summary
Brief summary (as posted)
Carfilzomib in combination with lenalidomide, daratumumab and dexamethasone (KRDd) can induce profound clinical responses. The investigators want to observe the effectiveness of the quadruple therapy of carfilzomib, lenalidomide, daratumumab and dexamethasone on patients receiving 8 cycles of KRDd with autologous stem cell transplantation versus patients with 8 cycles of KRDd without autologous stem cell transplantation.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Multiple Myeloma | Multiple Myeloma | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Daratumumab Only Product in Parenteral Dose Form | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Group A - Non transplant
- description
- Carfilzomib Lenalidomide Daratumumab Dexamethasone
- interventionNames
- Drug: Daratumumab Only Product in Parenteral Dose Form
- type
- ACTIVE_COMPARATOR
- label
- Group B - transplant
- description
- Carfilzomib Lenalidomide Daratumumab Dexamethasone Autologous stem cell transplantation (ASCT)
- interventionNames
- Drug: Daratumumab Only Product in Parenteral Dose Form
Primary outcomes (1)
- measure
- Complete response with negative minimal residual disease
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 65 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients with newly diagnosed and previously untreated multiple myeloma by the International Myeloma Working Group criteria that requires treatment based on: Presence of elevated calcium, renal failure, anemia and/or bone lesions (CRAB) Clonal bone marrow plasma cells ³ 60% Involved/uninvolved serum free light chain ratio ³ 100 \>1 focal lesions on MRI studies (³5 mm in size) 2. Age \> 18 years 3. Functional stage of 0 - 1 measured by the Eastern Cooperative Oncology Group (ECOG) scale. 4. Capacity and willingness to provide a written informed consent. Exclusion Criteria: 1. POEMS syndrome 2. Systemic amyloidosis 3. Plasma cells leukemia 4. Radiotherapy on multiple sites on the period of 4 weeks before the initiation of treatment (1 week if it is one region) 5. Improper liver function: total bilirubin \> 1.5 x upper limit of normal (ULN) or \> 3 x ULN in patients with Gilbert syndrome, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) \> 3.0 x ULN. 6. Non-controlled systematic active infection (viral, bacterial and/or fungic). 7. Patients with known infection by human immunodeficiency virus (HIV). 8. Active infection by hepatitis B. 9. Active infection by hepatitis C. 10. Significant cardiovascular diseases as uncontrolled or symptomatic arrhythmias, congestive heart failure or acute myocardial infarction within 2 months prior to screening, or any New York Heart Association (NYHA) class 3 or 4 heart disease. 11. Diagnosis of previous malignancies for 2 years, with exception of patients with basal or squamous cell carcinoma or "in situ" carcinoma of cervix or breast. 12. History of allergic reaction or severe anaphylaxis to humanized or murine monoclonal antibodies. 13. Pregnant or lactating women.
References
Publications (0)
Data not yet available
No reference posted for this study.