NCT04172467 · ADVERSE EVENTS
Adverse events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.
- Collection time frame
- 12 months
- Other-event reporting threshold
- 0%
Since this is an observational study of clinical routine, there is no studied medicinal product involved in this study and no safety event were extracted as part of this study.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Non-interventional Retropspective Observational Study. | 0 / 0 | 0 / 0 | 0 / 0 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- Since this is an observational study of clinical routine, there is no studied medicinal product involved in this study and no safety event were extracted as part of this study.
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 0
- description
- Data from 1086 patients (CLL 490, MM 596) were collected from 86 centres.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 0
- serious Num Affected
- 0
- serious Num At Risk
- 0
- title
- Non-interventional Retropspective Observational Study.
- frequency Threshold
- 0
- time Frame
- 12 months
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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