Interim safety analysis of a phase 2 randomized study of daratumumab (dara), lenalidomide (r), bortezomib (v), and dexamethasone (d; dara‐rvd) vs. rvd in patients (pts) with newly diagnosed multiple myeloma (mm) eligible for high‐dose therapy (hdt) and autologous stem cell transplantation (asct)
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Citation:
Blood vol 130 (suppl 1) 1879
Meeting Instance:
ASH 2017
Year:
2017
Type:
Abstract
Sub type:
Poster General
Funding:
AFT
Endpoint:
Secondary
Analysis:
Preliminary
Data Sharing:
No-Data-Sharing
Status:
Presented/Published
Citation Status:
ppub
Note:
Methodological:
No
Biospecimen:
No
SDC:
No
Parents:
None
Children:
3304  
Program:
OGC
Primary Committee:
Myeloma
Sec. Committees:
   
Pharmas:
Celgene, Takeda  
Grants:
 
Corr. Author:
 
Authors:
                           
Networks:
 
Study
AFT-29 (GRIFFIN)
Multiple Studies, or Legacy Studies in Alliance Study:
Phases:
2
Keywords: