NCT02002598 · OUTCOME
Number of Adverse Events (AEs)
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Adverse Events
- Interval / dispersion
- Not reported
- Time frame
- 30 Days Post Last Dose, Up to approximately 9 months
What was measured
Total number of AEs observed.
Groups in this outcome
CFZ With Bendamustine and Dexamethasone
All participants who received at least two cycles of CFZ either at 27mg/m\^2, 36mg/m\^2, 45 mg/m\^2, or 56mg/m\^2.
| Group | Source count |
|---|---|
| CFZ With Bendamustine and Dexamethasone | 20 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| CFZ With Bendamustine and Dexamethasone | 106 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 106
- denoms
- counts
- group Id
- OG000
- value
- 20
- units
- Participants
- description
- Total number of AEs observed.
- groups
- description
- All participants who received at least two cycles of CFZ either at 27mg/m\^2, 36mg/m\^2, 45 mg/m\^2, or 56mg/m\^2.
- id
- OG000
- title
- CFZ With Bendamustine and Dexamethasone
- param Type
- NUMBER
- reporting Status
- POSTED
- time Frame
- 30 Days Post Last Dose, Up to approximately 9 months
- title
- Number of Adverse Events (AEs)
- type
- SECONDARY
- unit Of Measure
- Adverse Events
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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